Showing results for: MLPA   Total: 5

  1. Kearns-Sayre syndrome (KSS)

    Analysis consists of identification of deletions and duplication in the mtDNA with use of ML…

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  2. Neurofibromatosis type 1 (NF1), von Recklinghausen disease

    Analysis consists of identification of large deletions or duplications involving the NF1 gen…

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  3. Hereditary neuropathy with liability to pressure palsy HNPP

    Analysis consists of quantitative testing of the exons 1 to 5 of the PMP22 gene with MLPA method

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  4. Telomery (badanie regionów subtelomerowych) test MLPA

    Quantitative analysis (detection of duplications-deletions) of the subtelomere regions for e…

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  5. Microdeletion (the most common arrangements of chromosome microdeletion) MLPA test

    Identified microdeletion/microduplication syndromes (all in single analysis): 1p36, 2p16, 3q…

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