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  1. *Jamsheer A, Sowińska A, Latos-Bieleńska A: A panel of genetic tests identifies causative mutation in around 40% of patients affected by bilateral syndromic and non-syndromic congenital limb malformations, International Congress of Human Genetics, Montreal, Kanada, 11-15.10.2011 Conference abstract book - poster 968F.
  2. K. Wiśniewska, A. Materna-Kiryluk, J. Mejnartowicz, A. Latos-Bieleńska and other members of the PRCM Working Group: Folic acid supplementation before and during pregnancy, 11  EUROCAT Symposium on Congenital Anomalies, Antwerp  14-18.06. 2011.
  3. *Wozniak A., D. Wolnik-Brzozowska, M. Wisniewska, R. Glazar, A. Materna-Kiryluk, T. Moszura, M. Badura-Stronka, J. Skolozdrzy, M. R. Krawczynski, J. Zeyland, W. Bobkowski, A. Latos-Bielenska, M. Szalata, R. Slomski, A., Siwinska. Frequency of 22q11.2 microdeletion in children with congenital heart defects in Western Poland. ESHG European Human Genetics Conference 2011, May 28 - 31, 2011, Amsterdam, The Netherlands. Abstracts Book, str. 84.
  4. *Dębicki S., M. Badura-Stronka, B. Budny, M. Wiśniewska, R. Glazar, A. Materna-Kiryluk, A. Jamsheer, E. Bonora, P. Magini,K.Männik, C.Graziano,A. Kurg,A. Latos-Bieleńska: SNP-array analysis in 64 Polish patients with intellectual disability – first results of the CHERISH project.  ESHG European Human Genetics Conference 2011, May 28 - 31, 2011, Amsterdam, The Netherlands. Abstracts Book, str. 134.
  5. Badura-Stronka M., W. Grotowski, B. Męczekalski, A. Wawrocka, K.Zawieja, M.R. Krawczyński, A. Latos-Bieleńska: Perrault syndrome in a female manifesting carrier of mtDNA 11778G>A mutation. ESHG European Human Genetics Conference 2011, May 28 - 31, 2011, Amsterdam, The Netherlands. Abstracts Book, str. 435.
  6. *Jamsheer A., A. Sowinska, A. Geppert, A. Latos-Bieleńska: Deletions of the GLI3 gene can be the frequent cause of Greig cephalopolysyndactyly and preaxial polydactyly type IV. ESHG European Human Genetics Conference 2011, May 28 - 31, 2011, Amsterdam, The Netherlands. Abstracts Book,  str. 94.
  7. Kalscheuer V.M., H. Hu, S. Haas, J. Chelly, H. Van Esch, M. Raynaud, S. G. M. Frints, A. de Brouwer, J. Gecz, S. Weinert, T. Zemojtel, M. Love, G. Froyen, F. Laumonnier, H. Richard, A. Emde, M. Bienek, C. Jensen, M. Hambrock, N. Lebrun, M. Corbett, C. Tan, C. E. P. van Rozendaa, M. Pocquet, N. Ronce, R. Sun, A. Hackett, M. Field, E. Haan, J. Nelson, G. Turner, G. Baynam, G. Gillessen-Kaesbach, U. Mueller, B. Budny, M. Badura-Stronka, A. Latos-Bieleńska, M. Cohen, T. Kleefstra, R. Ullmann, P. Wieacker, A. Dufke, G. R. Criado, M. Bondeson, H. van Bokhoven, A. Tzschach, K. Wrogemann, T. Jentsch, W. Chen, H. Ropers: Next-generation sequencing in >240 families with X-linked intellectual disability. ESHG European Human Genetics Conference 2011, May 28 - 31, 2011, Amsterdam, The Netherlands. Abstracts Book, str. 6.
  8. Jezela-Stanek A., E. Ciara, E. Małunowicz, K.Chrzanowska, A. Latos-Bieleńska, M.Krajewska-Walasek, SLOS Collaborative Group. Differences between predicted and established diagnoses of Smith-Lemli-Opitz syndrome in the Polish population : underdiagnosis or loss of affected fetuses? J.Inherit.Metab.Dis. 2010 : Vol. 33, nr 4, s. 458.
  9. Graziano C., Elena Bonora, P. Magini, J. Baptista, G. Tortora, S. Miccoli, P.C. Patsalis, J.A. Hettinger, V. Anastasiadou, L. Kousoulidou, A. Kurg, K. Männik, S. Parkel, O. Zilina, M. Nlukas, E. Öiglane-Silk, V. Kucinskas, J. Kasnauskiene, I. Lebedev, A. Latos-Bieleńska, M. Badura-Stronka, B. Budny, Z. Sedlacek, M. Havlovicova, M. Vickova, M. Hancarova, T. Sarkisian, D. Babikyan, S. Midyan, L.A. Livshits, A. Cuppoletti, G. Romeo: CHERISH - improving diagnoses of mental retardation in children in Eastern Europe and Central Asia through genetic characterisation and bioinformatics /statistics. European Human Genetics Conference 2010. Gothenburg, Sweden, June 12-15, 2010. - Eur. J. Hum. Genet. 2010 Vol. 18 suppl. 1 s. 86.
  10. Walczak-Sztulpa J., J. Eggenschwiler, D. Osborn, D. A. Brown, F. Emma, C. Klingenberg, R.C. Hennekam, G. Torre, M. Garshasbi, A. Tzschach, M. Szczepańska, M. Krawczyński, J.Zachwieja, Beales, H. Ropers, A. Latos-Bieleńska, A.W. Kuss: Cranioectodermal dysplasia is a ciliary disorder caused by defects in the IFT122 gene. European Human Genetics Conference 2010. Gothenburg, Sweden, June 12-15, 2010. - Eur. J. Hum. Genet. 2010 Vol. 18 suppl. 1 s. 26.
  11. Materna-Kiryluk A., Wiśniewska K., Mejnartowicz J., Latos-Bieleńska A., Wysocki J.,Wieckowska B., Borszewska-Kornacka M., Czerwionka-Szaflarska M., Gajewska E., Godula-Stuglik U., Krawczyński M., Limon J., Rusin J., Sawulicka-Oleszczuk H., Stańczyk J., Szwałkiewicz-Warowicka E., Walczak M.: Determinants of material periconceptional folic acid supplementation in Poland (Data from the Polish Registry of Congenital Malformations- PRCM). 1st European Congress “Preconception Care and Preconception health”, Bruksela 6-9.10.2010, Program&Abstract Book s. 123(P).
  12. Materna-Kiryluk A., Wiśniewska K., Mejnartowicz J., Latos-Bieleńska A., Wieckowska B., Balcar-Boron A., Borszewska-Kornacka M., Czerwionka-Szaflarska M., Gajewska E., Godula-Stuglik U., Krawczyński M., Limon J., Rusin J., Sawulicka-Oleszczuk H., Stańczyk J., Świetliński J., Szwałkiewicz-Warowicka E., Walczak M.: Congenital malformations in children delivered by women employed in agriculture and residing in rural areas. 1st European Congress “Preconception Care and Preconception health”, Bruksela 6-9.10.2010, Program&Abstract Book s. 112.
  13. Wiśniewska M., Walkowiak A., Materna-Kiryluk A., Latos- Bieleńska A.: Active genetic counseling as a way of preconception care on the basic of Polish Registry of Congenital Malformations (PRCM). 1st European Congress “Preconception Care and Preconception Health”, Bruksela 6-9.10.2010, s. 85.
  14. Latos-Bieleńska A.: Preconceptional care in Poland. Where are we now and where are we going?. 1st European Congress “Preconception Care and Preconception health”, Bruksela 6-9.10.2010, Program&Abstract Book str. 55.
  15. Sanna-Cherchi S., K.E. Burgess, M. Bodria, K. Kiryluk, V.J. Lozanovski, A. Materna-Kiryluk, V. Corbani, R. Sterken, N. Ristoska-Bojkovska, P.L. Weng, N. Kacak, G. Caridi, R.P. Lifton, L. Allegri, A. Latos-Bieleńska, Z. Gucev, F. Scolari, V. Tasic, G. M. Ghiggeri, A. G. Gharavi. A genome-wide screen for novel genomic disorders of the kidney and urinary tract development. W: Renal Week 2010. 43rd Annual Meeting & Scientific Exposition. Denver, Colorado, November 16-21, 2010. Abstracts. SA-FC383.
  16. Sanna-Cherchi S., Burgess K., Bodria M., Kiryluk K., Sterken R., Weng P.L., Kack N., Allergi L., Scolari F., R.P. Lifton, Latos- Bieleńska A., Tasic V., Ghiggeri G.M., Gharavi A.: Rare copy number variants in congenital anomalie of the kidney and urinary tract. The Fifteenth Congress of the International Pediatric Nephrology Association”,Pediatr. Nephrol. 2010 Vol 25 nr 9, s. 1911.
  17. Krajewska-Walasek M., A.Jezela-Stanek, E. Ciara, E. Małunowicz, M. Gajdulewicz, K.Spodar, A. Materna-Kiryluk, A. Pyrkosz, E. Obersztyn, J. Wierzba, R. Śmigieł, M. Kostuch, M. Pasińska, P. Socha, A. Dobrzańska, T. Michalska, A. Kutkowska-Kazimierczak, M. Orczyk, R. Glazar, L. Korniszewski, J. Zaremba, M. Wielgoś, L. Bablok, K. Chrzanowska, A. Latos-Bieleńska. Results of the Polish 3-year population surveillance program for Smith-Lemli-Opitz syndrome : Are so many patients missed or misdiagnosed? Eur.J.Hum.Genet. 2009 : Vol. 17 suppl. 2, s. 91.
  18. Sanna-Cherchi S., K. Kiryluk, S. Sanders, C. Izzi, M. Bodria, A[nna] Materna-Kiryluk, V. Corbani, A. Carrea, N. Kacak, G. Caridi, R. Sterken, M. State, R. Lifton, L. Allegri, A. Latos-Bieleńska, F. Scolari, M. Ghiggeri, A.G. Gharavi: Rare copy number variants in congenital anomalies of the kidney and urinary tract. ASN Renal Week. San Diego, CA, USA, October 27-November 1, 2009.J. Am. Soc. Nephrol. 2009 Vol. 20 Abstract Issue; s. 436A.
  19. Materna-Kiryluk A., K. Wiśniewska, A. Jamseer, M. Badura-Stronka, J. Mejnartowicz, B. Więckowska, A. Latos-Bieleńska: Epidemiological study of isolated, non-familial preaxial polydactyly type I: data from the Polish Registry of Congenital Malformations (PRCM), X Europejskie Sympozjum  EUROCAT “Prevention of Congenital Anomalies”, Bilbao, 10-12.06.2009, s. 76.
  20. *Latos-Bieleńska A.,  A. Jamsheer, A. Materna-Kiryluk, M. Badura-Stronka, K. Wiśniewska, and other members of PRCM Working Group: “Polish Registry of Congenital Malformations (PRCM) as a robust tool for studying molecular background of congenital malformations, X Europejskie Sympozjum  EUROCAT “Prevention of Congenital Anomalies”, Bilbao 10-12.06.2009, s. 82.
  21. K.Wiśniewska, A.Materna-Kiryluk, M.Badura-Stronka, J.Mejnartowicz,B.Więckowska,J.Wysocki, A. Latos-Bieleńska and other members of The PRCM Working Group: Folic acid supplementation and risk of isolated congenital malformations (Data from The Polish Registry of Congenital Malformations – PRCM), 1st Central and Eastern European Summit on Preconception Health and Prevention of Birth Defects,  Budapest, 27-30 August 2008, P-II/10, Program&Abstract Book, 160, 2008.
  22. M.Wiśniewska, M.Badura-Stronka, B.Brodecki, J.Richter, A.Materna-Kiryluk, J.Brzeziński, A. Latos-Bieleńska: Dysmorphology Platform – a web-based electronic system of dysmorphology consultation in Poland, 1st Central and Eastern European Summit on Preconception Health and Prevention of Birth Defects, Budapest, 27-30 August 2008,  P-II/9, Program&Abstract Book, 159, 2008.
  23. A.Materna-Kiryluk, A.Latos-Bieleńska, PRCM Working Group: Organization of The Polish Registry of Congenital Malformations,  1st Central and Eastern European Summit on Preconception Health and Prevention of Birth Defects: Budapest, 27-30 August 2008, P-I/10, Program&Abstract Book, 142, 2008.
  24. *A.Jamsheer, M.Badura-Stronka, A.Materna-Kiryluk, K.Wiśniewska, B.Więckowska,J.Mejnartowicz,A.Balcar-Boroń, M.Borszewska-Kornacka, M.Czerwionka-Szaflarska, E.Gajewska, U.Godula-Stuglik, M.Krawczyński, J.Limon, J.Rusin, H. Sawulicka-Oleszczuk, E.Szwałkiewicz-Warowicka, J.Świetliński, M.Walczak, A. Latos-Bieleńska: Amniotic Band Sequence With and Without Body Wall Complex: Clinical Characteristics Suggest Two Distinct Disease Entities, 1st Central and Eastern European Summit on Preconception Health and Prevention of Birth Defects,  Budapest, 27-30 August 2008, P-I/8, Program&Abstract Book, 140, 2008.
  25. Latos-Bieleńska A., A.Materna-Kiryluk, M.Wiśniewska, M.Badura-Stronka, A.Jamsheer, M.Krajewska-Walasek, J.Limon, T.Mazurczak  and other members of PRCM Working Group: Polish Registry of Congenital Malformations – benefit for medical genetics, 1st Central and Eastern European Summit on Preconception Health and Prevention of Birth Defects: “, Budapest, Hungary 27-30 August 2008,  Program&Abstract Book, 99, 2008.
  26. Latos-Bieleńska A., A.Materna-Kiryluk, J.P.Mejnartowicz, M.Badura-Stronka, K.Wiśniewska, B. Więckowska, M.Wiśniewska, M. Zakrzewska, R.Glazar and PRCM Working Group: Congenital malformations in children live born during 1998 – 2002 in Poland – data from The Polish Registry of Congenital Malformations (PRCM), 1st Central and Eastern European Summit on Preconception Health and Prevention of Birth Defects: “, Budapest, Hungary 27-30 August 2008, Program&Abstract Book, s. 97, 2008.
  27. Latos-Bieleńska A.: Birth defects in the Central and Eastern European region: morbidity, epidemiology, current activities. W: 1st Central and Eastern European Summit on Preconception Health and Prevention of Birth Defects. Budapest, Hungary, August 27-30, 2008. Program & Abstract Book. [B.m., 2008] s. 24.
  28. Latos-Bieleńska A.: Registries of congenital malformations – challenge and benefit for medical genetics, The Fifth International Symposium on Genetics, Health and Disease, Amristar/Indie, 17-19 February 2008.
  29. *Latos-Bieleńska A., J.Walczak-Sztulpa, M.Krawczyński, J.Zachwieja, D.Zwolińska: „Cranioectodermal Dysplasia (sensenbrenner’s syndrome) as an example of rare disease. Evolution of phenotypic features in two siblings”, 9th European Symposium „Prevention of Congenital Anomalies”, Naples, P1: 22, 2007.
  30. Latos-Bielenska A., A.Materna-Kiryluk, J.Mejnartowicz, K.Wiśniewska, M.Badura, A.Balcar-Boroń, B.Borszewska-Kornacka, G.Bręborowicz, M.Czerwionka-Szaflarska, A.Dobrzańska, J.Gadzinowski, E.Gajewska, U.Godula–Stuglik, E.Helwich, M.Krawczyński, J.Limon, H.Sawulicka-Oleszczuk, J.Oleszczuk, M.Piróg, J.Rusin, J.Stańczyk, E.Szwałkiewicz-Warowicka , J.Szczapa, J.Świetliński, M. Walczak: „Evaluation of  prenatal diagnosis of congenital malformations in Poland (2000-2005)”, „Prevention of Congenital Anomalies”9th European Sympodium,  Naples, C3:10, 2007.
  31. *Latos-Bieleńska A., J.Walczak-Sztulpa, M.Szczepańska, M.Krawczyński, J.Zachwieja, A.W. Kuss, H-H.Ropers, D. Zwolińska, A.Tzschach: „Cranioectodermal Dysplasia (sensenbrenner’s syndrome):report of two siblings”, 18 Jahrestagung der Deutschen Gesellschaft fur Humangenetik, Bonn, 7 -10.03.2007,  Medizinische Genetik, 19(1):77, P(56), 2007.
  32. Walczak-Sztulpa J., Wiśniewska M., Tzschach A., Menzel C., Kalscheuer V.M., Kuss A.W., Ropers H-H, Latos-Bieleńska A., Ullmann R.: „Detection of a 4.7 Mb deletion in 13q33.3.-q34 in a family with translocation t(12;13) and mental retardation by array-CGH”, ”,  18 Jahrestagung der Deutschen Gesellschaft fur Humangenetik, Bonn, 7 -10.03.2007. Medizinische Genetik, 19(1):82, P(76), 2007.
  33. Krajewska-Walasek M., L. Korniszewski, E. Ciara, E. Małunowicz, A. Jezela-Stanek, M. Gajdulewicz, K. Spodar, E. Popowska, A. Materna-Kiryluk, Krystyna Chrzanowska, A. Latos-Bieleńska. Smith-Lemli-Opitz syndrome - novel mutation with a mild phenotype. Eur.J.Hum.Genet. 2007 : Vol. 15 suppl. 1, s. 89-90.
  34. Czarny-Ratajczak M., K. Kozłowski, A. Latos-Bieleńska, D.J. Prockop: Compound heterozygous mutations in the diastrophic dysplasia sulfate transporter gene (DTDST) in a family with intermediate SEMD phenotype between MED and diastrophic dysplasia. Am.J.Hum.Genet., Suppl. 1762C, P:326, 2006.
  35. Czarny-Ratajczak M., K. Kozłowski, A. Latos-Bieleńska, D.J. Prockop: Two different autosomal dominant mutations in the MATN3 and COMP genes cause single early onset osteoarthritis with multiple epiphyseal dysplasia phenotype. Gene Therapy Research Symposium, Baton Rouge, P:46, 25.5.2006.
  36. Budny B., M. Wiśniewska, W. Chen, H. Omran, M. Fliegauf, A. Tzschach, L.R. Jensen, M. Badura, S. Lenzner, H.H. Ropers, A. Latos-Bieleńska: A novel X-linked mental retardation syndrome associated with primary ciliary dyskinesia and macrocephaly links cilia dysfunction to neurodevelopmental disorders. The 8th European Symposium "Prevention of Congenital Anomalies". Poznań, June 9-10, 2005. - Arch. Perinat. Med. 2005 supl. [właśc. Vol. 11 nr 2] s. 73 (też na s. 75).
  37. Mayer M., M. Mazurek-Grząbka, A. Latos-Bieleńska, V. Kalscheuer, M. Hoeltzenbein, H. Scherthan, H.H. Ropers: Complex translocation T(8,11,16) de novo in a patient with ectrodactyly and mental retardation. The 8th European Symposium "Prevention of Congenital Anomalies". Poznań, June 9-10, 2005. - Arch. Perinat. Med. 2005 supl. [właśc. Vol. 11 nr 2] s. 75.
  38. Wiśniewska M., M.R. Krawczyński, A. Latos-Bieleńska: Oculodentodigital syndrome - a case report. The 8th European Symposium "Prevention of Congenital Anomalies". Poznań, June 9-10, 2005. - Arch. Perinat. Med. 2005 supl. [właśc. Vol. 11 nr 2] s. 71.
  39. Buczyńska A., Z. Murowaniecki, S. Tarkowski, A. Materna-Kiryluk, A. Latos-Bieleńska: Spatial evaluation of birth defects and environmental hazards in Poland - pilot study. Poznań, June 9-10, 2005. - Arch. Perinat. Med. 2005 supl. [właśc. Vol. 11 nr 2] s. 47.
  40. Woźniak A., A. Siwińska, M. Godynicka, D. Wolnik-Brzozowska, J. Skołożdrzy, A. Materna-Kiryluk, M.R. Krawczyński, M. Wiśniewska, R. Glazar, A. Latos-Bieleńska, M. Wojtalik: 22q11.2 microdeletion as genetic background of congenital cardiac defects. The 8th European Symposium "Prevention of Congenital Anomalies", Poznań, 9-10.06.2005. Archives of Perinatal Medicine, Suppl., 49, 2005.
  41. Buczyńska A., Z. Murowaniecki, S. Tarkowski, A. Materna-Kiryluk A. Latos-Bieleńska: Spatial evaluation of birth defects and environmental hazards in Poland - pilot study. The 8th European Symposium "Prevention of Congenital Anomalies", Poznań, 9-10.06.2005. Archives of Perinatal Medicine, , Suppl.,47, 2005.
  42. Walczak M., T. Zimoń, M. Giżewska, Z. Celewicz, M. Makowski, D. Subicka, H. Chrystyniak, E. Gawrych, E. Baryła-Pankiewicz, S. Zajączek, I. Staroniewska, A. Walczak, E. Ronin-Walknowska, J. Rudnicki, R. Czajka, J. Patalan, A. Romanowski, J. Mejnartowicz, A. Materna-Kiryluk, A. Latos-Bieleńska: Prevelance and type of congenital defects among infants born in western Pomeranian district in the years 1998-1999. The 8th European Symposium "Prevention of Congenital Anomalies", Poznań, 9-10.06.2005. Archives of Perinatal Medicine, Suppl.,44, 2005.
  43. Kossakowska-Krajewska A., E. Szwałkiewicz-Warowicka, A. Materna-Kiryluk, K. Wiśniewska, J. Mejnartowicz, G. Sorbaj-Sucharska, A. Latos-Bieleńska: Congenital malformations of newborns in the Olsztyn province in 1998 and the Warmia-Mazury province (1999-2000) incidence and epidemiological analysis. The 8th European Symposium "Prevention of Congenital Anomalies", Poznań, 9-10.06.2005. Archives of Perinatal Medicine,  Suppl., 43,2005.
  44. Mejnartowicz J., A. Materna-Kiryluk, M. Czerwionka-Szaflarska, M. Krawczyński, A. Latos-Bieleńska: Neural tube defects prevalence in three regions of western Poland in 1997-2000. The 8th European Symposium "Prevention of Congenital Anomalies", Poznań, 9-10.06.2005. Archives of Perinatal Medicine, Suppl., 36,2005.
  45. Ksionski S., A. Materna-Kiryluk, K. Wiśniewska, J. Mejnartowicz, A. Balcar-Boroń, M. Czerwionka-Szaflarska, E. Gajewska, M. Krawczyński, J. Limon, J. Rusin, H. Sawulicka-Oleszczuk, J. Stańczyk. E. Szwałkiewicz-Warowicka, J. Świetliński, M. Walczak, J. Wierzba, A. Latos-Bieleńska: Hydrocephaly and microcephaly in children born between 1998-2002 in Poland and California - epidemiological studies. The 8th European Symposium "Prevention of Congenital Anomalies", Poznań, 9-10.06.2005. Archives of Perinatal Medicine, Suppl., 35, 2005.
  46. Matema-Kiryluk A., K. Wiśniewska, J. Mejnartowicz, A. Balcar-Boroń, M.Czerwionka-Szaflarska, E. Gajewska, U. Godula-Stuglik, M. Krawczyński, J Limon, J. Rusin, H. Sawulicka-Oleszczuk. J. Stańczyk, E. Szwałkiewicz-Warowicka, J. Świetliński, M. Walczak, K. Kamiński, A. Latos-Bieleńska: Maternal age as a risk factor for isolated congenital malformations in children identified by the Polish Registry of Congenital Malformations. The 8th European Symposium "Prevention of Congenital Anomalies", Poznań, 9-10.06.2005. Archives of Perinatal Medicine, Suppl.,34,2005.
  47. Krawczyński M.R., and Working Group of PRCM:, A. Materna-Kiryluk, J. Mejnartowicz, A. Balcar-Boroń, M. Czerwionka-Szaflarska, E. Gajewska, M. Krawczyński, J. Limon, J. Stańczyk, E. Szwałkiewicz-Warowicka, M. Walczak, A. Latos-Bieleńska: Congenital malformations of the organ of vision: epidemiological data based on Polish Registry of Congenital Malformations 1997-2001, diagnostic recommendations and genetic counselling. The 8th European Symposium "Prevention of Congenital Anomalies”, Poznań, 9-10.06.2005. Archives of Perinatal Medicine, Suppl.,14,2005.
  48. Posmyk R., B. Panasiuk, A. Latos-Bieleńska, D. Wolnik-Brzozowska, M. Piotrowicz, V. Kucinskas, L. Korniszewski, B. Kozak-Klonowska, G. Sorbaj-Sucharska, A.T. Midro: A quantitative definition of monosomy 5p syndrome. European Human Genetics Conference 2005. May 7-10, 2005, Prague, Czech Republic. - Eur. J. Hum. Genet. 2005 Vol. 13 suppl. 1 s. 117.
  49. Budny, W. Chen, M. Wiśniewska, M. Hoeltzenbein, M.Badura, A. Tzschach, A. Latos-Bieleńska, H.H. Ropers, S. Lenzner. A new XLMR syndrome characterized by mental retardation, primary ciliary dyskinesia and macrocephaly, caused by a novel mutation in OFD1. 16. Jahrestagung der Deutschen Gesellschaft für Humangenetik gemeinsam mit der Österreichischen Gesellschaft für Humangenetik und der Schweizerischen Gesellschaft für Medizinische Genetic. Halle/Saale, Germany, 9-12 March 2005. - Med. Genet. 2005 Jg. 17 nr 1 s. 42.
  50. Budny B., W. Chen, M. Wiśniewska, A. Tzschach, H. Omran, M. Fliegauf, M. Badura, L.R. Jensen, M. Raynaud, A. Latos-Bieleńska, S. Lenzner, H.H. Ropers. A new XLMR syndrome characterized by mental retardation, primary ciliary dyskinesia and macrocephaly, caused by a novel mutation in OFD1. European Human Genetics Conference 2005. May 7-10, 2005, Prague, Czech Republic.  - Eur. J. Hum. Genet. 2005 Vol. 13 suppl. 1 s. 65-66.
  51. Budny B.,W. Chen, M.Badura, M. Hoeltzenbein, M. Wiśniewska, A.Tzschach, A. Materna-Kiryluk, A.Latos-Bieleńska, H.H. Ropers, S. Lenzner. Two new loci for non-syndrome X-linked mental retardation (MRX) map to Xq22-1-Xq22.3 and Xq23-Xq26.1. 16. Jahrestagung der Deutschen Gesellschaft für Humangenetik gemeinsam mit der Österreichischen Gesellschaft für Humangenetic und der Schweizerischen Gesellschaft für Medizinische Genetic. Halle/Saale,Germany, 9-12.3.2005. Med. Genet. 2005 Jg. 17 nr 1 s. 99.
  52. Czarny-Ratajczak M., A. Kołczewska, A. Woźniak, A. Latos-Bieleńska, I. Zimmermann-Górska, D.J. Prockop: High frequency of the MATN3 gene mutation in patients with osteoarthritis from the Polish population. Gene Therapy Research Symposium, P41,67-68, 2005.
  53. Czarny-Ratajczak M., A. Latos-Bieleńska, J. Sulko, K. Kozłowski, D.J. Prockop: Novel amino acid substitution in the Y - position of collagen type II causes spondyloepimetaphyseal dysplasia congenita. Gene Therapy Research Symposium, P38,66, 2005.
  54. Czarny-Ratajczak M., A. Kolczewska, A. Wozniak, A. Latos-Bielenska, I. Zimmermann-Gorska, D. J. Prockop. High frequency of the MATN3 gene mutation in patients with osteoarthritis. 55th Annual Meeting of American Society of Human Genetics, Salt Lake City, Utah, October 25-29, 2005. Am. J. Hum. Genet.,Suppl. 2005, p. 364.
  55. Czarny-Ratajczak M., Piotr Rogala, A. Latos-Bielenska, L. Ala-Kokko: Exclusion of candidate genes in four families with autosomal dominant multiple epiphyseal dysplasia from the Polish population. (A42) . Sixteenth Annual Tulane Health Sciences Research Days, New Orleans, 28-29.04.2004 (abstract: A42).
  56. Mayer M., Wiśniewska M., Kołowska J., Hoeltzenbein M., Latos-Bieleńska A., Ropers H.H., Kalscheuer V.M.: Disruption of the glutamate transporter gene EAAT2 in a boy with mental retardation, epilepsy and t(1;11)(p33;p13) translocation. European Human Genetics Conference, Monachium-Niemcy, 12-15.06.2004. Eur.J.Hum.Genet. 12, Suppl. 1: 142, 2004.
  57. Budny B., Badura M., Chen W., Hoeltzenbein M., Wiśniewska M., Tzschach A., Materna-Kiryluk A., Glazar R., Kalscheuer V.M., Latos-Bieleńska A., Ropers H.H., Lenzner S.: Examination of XLMR families by linkage analysis using SNPs and mutation screening in candidate genes. Max-Planck-Institute for Molecular Genetics, Day of Science, Berlin, 25.02.2004.
  58. Budny B., Wiśniewska M., Hoeltzenbein M., Badura M., Chen W., Mazurek M., Latos-Bieleńska A., Ropers H.H., Lenzner S.: A novel family with X-linked mental retardation, primary ciliary dyskinesia (PCD) and macrocephaly, linked to Xp22.32-Xp21.3. European Human Genetics Conference, Monachium – Niemcy, 12-15.06.2004. Eur.J.Hum.Genet. 12, Suppl.1: 284, 2004.
  59. Tzschach A., M. Hoeltzenbein, I. Bache, S. Tinschert, C. Bommer, H. Korner, G. Thiel,J. Musebeck, T. Grimm, E. Henn, e. Brude, M. Kruger, B. Leube, B. Schulze, G. Schwanitz,R. Raff, A. Dufke, G.Wolff, A. Latos-Bieleńska, S. Ebner, M. Kossakiewicz, S. Fuchs, G. Barbi, A. Kohler, D. Wand: Late-onset diseases among arriers of balanced chromosome rearrangements – esults of a multicentre survey. Eur.J.Hum.Genet. 12:133-134, 2004.
  60. Latos-Bieleńska A., Materna-Kiryluk A., Mejnatrowicz J.P., Wiśniewska M.: Results of response of families at risk to the information on genetic counselling – data from the Polish Registry of Congenital Malformation (PRCM). 7th European Symposium on the Prevention of Congenital Anomalies, Heildelberg – Niemcy, 30.05.2003, mat. zjazd. str.141.
  61. Łącka K., A. Rzepka, J. Andrzejewska, A. Wojda, A. Latos-Bieleńska: Fertility in Turner syndrome. 6th European Congress of Endocrinology. Lyon, France, 26-30 April 2003. mat.zjazd. P0763.
  62. Czarny-Ratajczak M., P. Rogala, A. Latos-Bieleńska, L. Ala-Kokko: Exclusion of candidate genes in four families with autosomal dominant multiple epiphyseal dysplasia. 53rd Annual Meeting of American Society of Human Genetics, Los Angeles, November 4-8, 2003. Am. J. Hum. Genet.  2003 (abstract: A2205)
  63. Zawirska A., A. Materna-Kiryluk, J. Mejnartowicz, M. Krawczyński, E.Gajewska, M. Walczak, A. Balcar-Boroń, M. Czerwionka-Szaflarska, J. Limon, E. Szwałkiewicz-Warowicka, U. Godula-Stuglik, K. Kamiński, J. Swietlinski, B. Raszeja-Kotelba, A. Latos-Bieleńska. The incidence and types of congenital malformations of the skin and appendages in Polish population. Abstracts of the 11th Congress of the European Academy of Dermatology & Venereology. 2-6 October 2002, Prague, Czech Republic. - J. Eur. Acad. Dermatol. Venereol. 2002 Vol. 16 suppl. 1 s. 219.
  64. Latos-Bieleńska A.: Polish Registry of Congenital Malformations. VI European Symposium on Prevention of Congenital Anomalies, Catania – Włochy, 1-4.06.2001.
  65. Krawczyński M.R., A. Gotz-Więckowska, M. Krawczyński, Latos-Bieleńska A.: Congenital eye malformations in children born in western Poland 1997-1999. XIII Congress of the European Society of Ophthalmology, Instanbul-Turcja, 3-4 June 2001, mat.zjazd. 137.
  66. Słopień A., A.Rajewski, B. Budny, P.Czerski, J.Hauser, A. Latos-Bieleńska, A. Kochański: Chromosomal aberrations in autistic disorder. World Federation of Societies of Biological Psychiatry. 7th World Congress of Biological Psychiatry, 1-6 July, 2001, Berlin, Germany. World J. Biol. Psychiatry  Vol. 2,1:210S, 2001.
  67. Czerski P., J. Hauser, M. Czarny-Ratajczak, P. Kapelski, S. Godlewski, F. Rybakowski, M. Dmitrzak, A. Latos-Bieleńska, J. Rybakowski. No association between DRD3 gene BalI polymorphism and schizophrenia. Eighth World Congress on Psychiatric Genetics. Versailles, France, 27-31 August, 2000. Abstracts of Presentations.- Am. J. Med. Genet. 2000 Vol. 96 nr 4 s. 529.
  68. Kochański A., Jędrzejowska H., Ryniewicz B., Barciszewska A.M., Lofgren A., Timmerman V., De Jonghe P., Czarny-Ratajczak M., Samocko J., Latos-Bieleńska A., Hausmanowa-Petrusewicz I.: X-dominant Charcot-Marie-Tooth disease with a novel E208G cx32 gene mutation. 5th Congress of the European Federation of Neurological Sciences, Copenhagen, 14-18.10.2000.
  69. Walczak M., Fydryk J., Gawrych E., Dawid G., Pankiewicz E., Zajączek S., Rudnicki J., Walczak A., Subicka D., Materna-Kiryluk A., Latos-Bieleńska A.: Congenital defects – an aggravating problem in contemporary pediatrics? (Preliminary report). European Congress of Paediatrics 2000, Rzym, 18-21.03.2000, mat.zjazd. str. 109.
  70. Kossakowska-Krajewska A., Szwałkiewicz-Warowicka E., Mejnartowicz J., Materna-Kiryluk A., Latos-Bieleńska A.: The incidence of congenital malformations in Olsztyn district (Poland) in 1998. XVII European Congress of Perinatale Medicin Porto, Portugal, 25 – 28.06.2000. Prenatal and Neonatal Medicine 5 (Suppl. 2):133, 2000.
  71. Latos-Bieleńska A., Materna-Kiryluk A., Krawczyński M.R., Mejnartowicz J.P., Krawczyński M., Gajewska E., Limon J., Balcar-Boroń A., Walczak M., Stańczyk J.: Congenital malformations in Poland - data from the Polish Registry of Congenital Malformations. 38th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), Warszawa, 29.08.-01.09.1999. Hormone Research, 51 (Suppl. 2), 78, 1999.
  72. Krawczyński M.R., Czarny-Ratajczak M., Pecold K., Latos-Bieleńska A.: Molecular background of Marshall syndrome in patients from Polish population. XIIth Congress of the European Society of Ophthalmology, Stockholm,  Sweden, 27.06.-01.1999. Ophthalmic Research, 31 (Suppl. 1), 95, 1999.
  73. Krawczyński M.R., Czarny-Ratajczak M., Pecold K., Latos-Bieleńska A.: Molecular background of Marshall syndrome in patients from Polish population. European Association for Vision and Eye Research - Joint European Research Meeting in Ophthalmology and Vision, Palma de Mallorca, 6-9.10.1999. Ophthalmic Res. 1999 Vol. 31 suppl. 1 s. 95.
  74. Czarny-Ratajczak M., Rogala P., Annunen S., Ala-Kokko L., Latos-Bieleńska A.: Analysis of the COMP, COL9A1, COL9A2, COL9A3 genes in patients with multiple epiphyseal dysplasia from the Polish population. 31st Annual Meeting of the Eur. Soc. Hum. Genet., Geneva, 29.05.-1.06.1999. Eur.J.Hum.Genet. 7 (Suppl.1), 118, 1999.
  75. Mejnartowicz J., Czyżewska M., Materna-Kiryluk A., Krawczyński M., Balcar-Boroń A., Limon J., Gajewska E., Walczak M., Stańczyk J., Szwałkiewicz E., Krawczyński M.R., Wiśniewska M., Glazar R., Wolnik-Brzozowska D., Błońska-Polarczyk B., Ignyś A., Latos-Bieleńska A.: Neural tube defects: main epidemiological features - a population based study from Polish Registry of Congenital Malformations (PRCM). 31st Annual Meeting of the Eur. Soc. Hum. Genet., Geneva, 29.05.-01.06.1999. Eur.J.Hum.Genet. 7 (Suppl. 1), 61, 1999.
  76. Latos-Bieleńska A., Materna-Kiryluk A., Mejnartowicz J.P., Krawczyński M., Balcar-Boroń A., Limon J., Gajewska E., Walczak M., Stańczyk J., Szwałkiewicz E., Krawczyński M.R., Wiśniewska M., Glazar R., Wolnik-Brzozowska D., Błońska-Polarczyk B., Ignyś A.: Polish Registry of Congenital Malformations - the improvement of identification of malformed children and the genetic care in their families. 31st Annual Meeting of the Eur. Soc. Hum. Genet., Geneva, 29.05.-01.06.1999. Eur.J.Hum.Genet. 7 (Suppl. 1), 60, 1999.
  77. Kochański A.,  Mejnartowicz J.,  Latos-Bieleńska A., Etienne J., Filipczyński L.: Double-strand DNA damage by litotripter generated shock waves. Forum Acusticum 1999. Berlin, March 14-19, 1999 jointly held with ASA and DEGA. Acta Acustica 85 (Suppl. 1), 307, 1999.
  78. Czarny M., Rogala P., Kołodziej Ł., Latos-Bieleńska A.: Mutation analysis of the COL2A1, COL9A1 and COL9A2 genes in patients with the type II collagenopathies and multiple epiphyseal dysplasia. (p.106) IUBMB Conference of Health and Diseases,  Jerusalem, 18-22.10.1998, mat.zjazd.str. 106.
  79. Ignyś A., Głowacki M., Latos-Bieleńska A.: Diagnostic difficulties in brachyolmia – presentation of two cases. XXII International Congress of Pediatrics, Amsterdam 9-14.08.1998, mat.zjazd. str.225.
  80. Latos-Bieleńska A., Materna-Kiryluk A., Krawczyński M.R., Krawczyński M., Limon J, Balcar-Boroń M., Gajewska E., Walczak M., Stańczyk J., Szymański W., Mejnartowicz J., Wiśniewska M., Wolnik-Brzozowska D., Glazar R., Ignyś A., Błońska-Polarczyk B.: Polish Registry of Congenital Defects: a source for epidemiological research and application to improvement of genetic care for families at risk. XXII International Congress of Pediatrics, Amsterdam 9-14.08.1998 mat.zjazd, str.368.
  81. Wiśniewska M., Wolnik-Brzozowska D., Glazar R., Krawczyński M.R., Latos-Bieleńska A.: Regional Registry of Congenital Defects as an important factor of improvement of genetic care for families at risk. XXII International Congress of Pediatrics, Amsterdam 9-14.08.1998, mat.zjazd. str.365.
  82. Kochański A., V.Timmerman, A. Löfgren, V. Wouters, E. De Vriendt, J. Jaruzelska, B. Ryniewicz, H. Jędrzejowska, C. Van Broeckhoven, A. Latos-Bieleńska, I.Hausmanowa-Petrusewicz. Molecular genetic analysis of Charcot-Marie-Tooth patients in Poland. : Report and abstracts of the 7th Annual Symposium of the European Chacot-Marie-Tooth Consortium. Antwerpen, Belgium, July 3-5, 1998. - J. Peripher. Nerv. Syst. 1998 Vol. 3 nr 4 s. 294-295.
  83. Krawczyński M.R., M. Wiśniewska, A. Latos-Bieleńska. Consciousness of genetic risk and demand for genetic counselling in families of children with birth defects. Abstracts from the 9th Asian Congress of Paediatrics. Hong Kong, 23rd - 27th March 1997. - J. Paediatr. Child Health 1997 Vol. 33 suppl. 1 s. S104.
  84. Zawada M., M. Jarmuż, A. Wojda, J. Kołowska, M. Mazurek, A. Latos-Bieleńska. A cytogenetic and FISH studies of the autosome marker chromosomes. Abstracts of the 1st European Cytogenetics Conference. Athens, Greece, June 22-25, 1997. - Cytogenet. Cell Genet. 1997 Vol. 77 nr 1-2 s. 68.
  85. Latos-Bieleńska A., R. Glazar, M. Jungerman, J. Kołowska, M. Wiśniewska, M. Zawada. UPD14 or hidden mosaicism 14 - an important problem for genotype-phenotype correlation. Abstracts of the 1st European Cytogenetics Conference. Athens, Greece, June 22-25, 1997. - Cytogenet. Cell Genet. 1997 Vol. 77 nr 1-2 s. 113.
  86. Wojda A., J. Kołowska, M. Zawada, M. Jarmuż, K. Łącka, M. Krawczyński, A.Latos-Bieleńska.Significance of FISH in precise cytogenetic diagnostics in Turner syndrome patients. Abstracts of the 1st European Cytogenetics Conference. Athens, Greece, June 22-25, 1997. - Cytogenet. Cell Genet. 1997 Vol. 77 nr 1-2 s. 67.
  87. Wojda A., J. Kołowska, M. Jarmuż, M. Zawada, M. Mazurek, M. Krawczyński, K. Łącka, A.Latos-Bieleńska. Clinical recognition of Turner syndrome and chromosomal aberrations. 29th Annual Meeting of The European Society of Human Genetics. Genua, Italy, May 17-20, 1997.- Med. Genet. 1997 Vol. 9 Nr 2 suppl. s. 79.
  88. Zawada M., M. Jarmuż, A. Wojda, J. Kołowska, M. Mazurek, A.Latos-Bieleńska. Identification of additional marker chromosomes by fluorescence in situ hybridization. 29th Annual Meeting of The European Society of Human Genetics. Genua, Italy, May 17-20, 1997.- Med. Genet. 1997 Vol. 9 Nr 2 suppl. s. 80.
  89. Latos-Bieleńska A., M. Zawada, D. Wolnik-Brzozowska, J. Kołowska, A. Wojda, M. Jarmuż, M.R. Krawczyński. Comparison of phenotypes of duplication or deletion of the same fragment of chromosome 13: 13(q31.2q33.1). 29th Annual Meeting of The European Society of Human Genetics. Genua, Italy, May 17-20, 1997.- Med. Genet. 1997 Vol. 9 Nr 2 suppl. s. 70.
  90. Kusz K., R.Matuszak, M. Szarras-Czapnik, A. Wojda, A. Latos-Bieleńska, A. Ruszczyńska-Wolska, M. Kotecki, J. Jaruzelska. Genotype-phenotype correlation in (Y+) XX males and (Y+) XX true hermaphrodites. 29th Annual Meeting of The European Society of Human Genetics. Genua, Italy, May 17-20, 1997.- Med. Genet. 1997 Vol. 9 Nr 2 suppl. s. 158.
  91. Kusz K., R.Matuszak, M. Szarras-Czapnik, A. Wojda, A. Latos-Bieleńska, A. Ruszczyńska-Wolska, M. Kotecki, J. Jaruzelska. Genotype-phenotype correlation in (Y+) XX males and (Y+) XX true hermaphrodites. 29th Annual Meeting of The European Society of Human Genetics. Genua, Italy, May 17-20, 1997.- Med. Genet. 1997 Vol. 9 Nr 2 suppl. s. 158.
  92. Harabasz A., M. Głowacki, M.R. Krawczyński, A. Szulc, D.Wolnik-Brzozowska, M. Wiśniewska, R. Glazar, M. Krawczyński, A. Latos-Bieleńska. Diagnostic problems in Marfan syndrome patients. 29th Annual Meeting of The European Society of Human Genetics. Genoa, Italy, May 17-20, 1997.- Med. Genet. 1997 Vol. 9 Nr 2 suppl. s. 28.
  93. Wolnik-Brzozowska D., Wiśniewska M., Krawczyński M.R., Latos-Bieleńska A.: Primary and secondary preventive methods of congenital abnormalities - evaluation of the stage in Poland. 29th Annual Meeting of the Eur. Society of Human Genetics, Genua, 17-20.05.1997. Med. Genet. 1997 Vol. 9 Nr 2 suppl. s. 62.
  94. M.R. Krawczyński, M. Wiśniewska, R. Glazar, D.Wolnik-Brzozowska, A. Latos-Bieleńska: Consciousness of genetic risk and demand for genetic counselling in families of children with congenital defects. 29th Annual Meeting of The European Society of Human Genetics. Genua, Italy, May 17-20, 1997. - Med. Genet. 1997 Vol. 9 Nr 2 suppl. s. 51.
  95. Zawada, A.Latos-Bieleńska, D.Brzozowska, J.Kołowska, A.Wojda, M.Jarmuż, M.R.Krawczyński: The phenotype of children with duplication or deletion 13(q31.2q33.1). Jahrestagung der Gesellschaft fur Humangenetik, Goettingen, 06-09.03.1996. Medizinische Genetik 1, 76, 1996.
  96. Krawczyński M.R., M.Wiśniewska, R.Glazar, D.Wolnik-Brzozowska, A.Latos-Bieleńska: The manner of informing about birth of child with congenital defects - genetic risk families' point of view. Annual Meeting of the Eur. Soc. Social Pediatrics, Milano, 7-10.11.1996, s. 257.
  97. Łącka K., J.Kosowicz, A. Wojda, A. Czarnywojtek, A.Latos-Bieleńska. Numerical and structural chromosome X aberrations and clinical features in patients with Turner syndrome. XV Congress of the Polish Society of Endocrinology in cooperation with the European Federation of Endocrine Societies. Poznań, Poland, May 19-23, 1996. - J. Endocrinol. Invest. 1996 Vol. 19 nr 3 suppl. s. 31.
  98. Krawczyński M.R., W.Just, W.Vogel, A.Latos-Bieleńska: Nance-Horan syndrome – looking for microdeletion. 21. International Congress of Pediatrics, Cairo, 10-15.09.1995, s. 448.
  99. Zawada M., K. Chrzanowska, H. Hameister, Ch. Klett, M. Krajewska-Walasek, A.Latos-Bieleńska. Identification of a marker chromosome as der(15), t(15:16)(pter-q12::q22-qter) in a 1 year old girl by FISH. 27th Annual Meeting of the European Society of Human Genetics. 7th Annual Meeting of the Society of Human Genetics in Germany. Berlin, 23-27 May, 1995. - Med. Genet. 1995 Jg. 7 nr 2 s. 237.
  100. Zawada M, A. Wojda, D. Wolnik-Brzozowska, J. Kołowska, M. Jarmuż, P. Fichna, P. Kądziołka, A. Warenik, A. Latos-Bieleńska: Cytogenetic and ISH studies in patients with disturbances of sex determination. The 6th Annual Meeting of the German Society of Human Genetics. Düsseldorf, 23-26 March 1994. - Med. Genet. 1994 Jg. 6 nr 1 s. 116.
  101. M.R. Krawczyński, M. Skowrońska, R. Glazar, A. Latos-Bieleńska: A case of Nance-Horan syndrome with mental retardation and neurological signs.  The 6th Annual Meeting of the German Society of Human Genetics. Düsseldorf, 23-26 March 1994. - Med. Genet. 1994 Jg. 6 nr 1 s. 104.
  102. Szewierski Z., J.Markowska, A. Latos-Bieleńska: Przypadek rodzinnego występowania chrzęstniaka w tkankach miękkich. IX Konferencja Naukowo-Szkoleniowa pt. "Chemioterapia guzów tkanek miękkich" Sekcji Chemioterapii Polskiego Towarzystwa Onkologicznego. Kiekrz k. Poznania, Poznań, 24-25 IX 1993. mat.zjazd. str. 52-53.
  103. Latos-Bieleńska A., K.Bombicki, J.Wronka, M.Witt: Clinical and EMG studies in family with Charcot-Marie-Tooth disease type I. Klinik, Pathogenese und Genetik Neuromuskularer Erkrankungen, Wurzburg 29.9-2.10.1993.
  104. Krawczyński M., A.Latos-Bieleńska: Identification of genetic risk families and genetic counselling of congenital defects. Congress of European Society of Social Pediatrics, Bern, 15-19.10.1991.
  105. Krawczyński M.R., J.Walkowiak, A.Wojda, A.Latos-Bieleńska: BrdU-antibody technique in diagnosis of structural  chromosome aberrations. 3. Tagung der Gesellschaft f. Humangenetik, Ulm, 10-13.4.1991, mat.zjazd. str.186.
  106. Kotecki M., A.Latos-Bieleńska, M.Skowrońska, P.Fichna, A.Marcinkowska, J.Jaruzelska: Non-isotopic in situ hybridization and molecular studies of patients with Y chromosome aberrations. 3. Tagung der Gesellschaft f. Humangenetik, Ulm, 10-13.4.1991, mat.zjazd str.340.
  107. Vogel W., A.Latos-Bieleńska, W.Just: The BrdU antibody technique (BAT) - an approach to chromosome replication. 3.Tagung der Gesellschaft f. Humangenetik, Ulm, 10-13.4.1991, mat.zjazd str.98.
  108. Wolnik-Brzozowska D., A.Latos-Bieleńska: The Wiedemann-Rautenstrauch syndrome and features of connective tissue disorder in two sisters. 3. Tagung der Gesellschaft f. Humangenetik, Ulm, 10-13.4.1991, mat.zjazd str.149.
  109. Latos-Bieleńska A., J.Limon, W.Vogel: Visualization of lateral asymmetry in human metaphase chromosomes using a BrdU-antibody techniqueBAT). 2.Tagung der Gesellschaft fur Humangenetik, Bonn, 28-31.03.1990, mat.zjazd. str. 158.
  110. Kołowska J., A.Wojda, A.Latos-Bieleńska: Reciprocal translocation 2q;17q in father and son resulted in a deletion 17q23.3-q24.2 in the son. 1.Tagung der Gesellschaft fur Humangenetik, Monachium, 4-8.04.1989, mat.zjazd.str.290.
  111. Skowrońska M,., H.Hameister, A.Latos-Bieleńska: Partial trisomy 22 - cytogenetic and ISH studies. 1.Tagung der Gesellschaft fur Humangenetik, Monachium, 4-8.04.1989, mat.zjazd. str.284.
  112. Latos-Bieleńska A., W.Vogel: BrdU-antibody technique in meiosis: preliminary results from light and electron microscopy. 1.Tagung der Gesellschaft fur Humangenetik,  Monachium, 4-8.04.1989, mat.zjazd str.251.
  113. Latos-Bieleńska A.: Bird-headed" mental retardation syndrome in two brothers. 3rd Manchester Birth Defects Conference, Manchester, 25-28.10.1988.
  114. Latos-Bieleńska A., D.Wolnik-Brzozowska, M.Wiśniewska: Organization, effectivity and psychosocial aspects of active genetic counselling in West Poland. 1. Eur. Meeting on Psychosoc. Aspects of Genet. Counselling, Groningen, 9-11.11.1988, mat.zjazd.str 131.
  115. Engel M.,  A.Latos-Bieleńska, H.Hameister: Konservierte Chromosomenbereiche im Genom der Sauger. 20.Tagung der Gesellschaft  fur Anthropologie und Humangenetik, Giessen, 30.9-3.10.1987, mat.zjazd str.229.
  116. Latos-Bieleńska A., E.Sobkowiak, A.Marcinkowska: Presumably new autosomal recessive malformation syndrome with phenotype of 13q. 20.Tagung der Geselllschaft  fur Anthropologie und Humangenetik, Giessen, 30.9-3.10.1987, mat.zjazd str. 135.
  117. Słomski R., A.Latos, J.Jaruzelska: Studies of interaction of homologous RNA with normal mouse lymphocytes. Światowy Zjazd Genetyczny, Moskwa, 1978.
  118. Słomski R., A.Latos, J.Jaruzelska, M.Labuda: Studies of interaction of immune RNA with normal mouse lymphocytes. 4th European Immunology Meeting, Budapeszt, 1978.
  119. Latos A., R.Słomski, M.Labuda: Comparison of incorporation of immune RNA by normal and immunized mouse spleen cells. 12th FEBS Meeting, Drezno, 1978.
  120. Słomski R., J.Jaruzelska, W.M.Stolzmann, K.Wiktorowicz,  A.Latos: Small nuclear RNAs in lymphocytes stimulated with mitogen and antigen. 12th FEBS Meeting, Drezno, 1978.
  121. Latos A., R.Słomski, A.Horst: Studies on the interaction of immune RNA with normal spleen cells. 11th FEBS Meeting, Copenhagen, 1977.
  122. Latos A., R.Słomski: The comparison of incorporation by normal spleen cells of informational and control RNA from mouse spleen cells. 3rd European Immunology Meeting, Copenhagen 1976.