Showing results for: niedobór wzrostu   Total: 7

  1. Cohen Syndrome

    Sequencing analysis of exon 23 of COH1 gene (common mutation)

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  2. Feingold Syndrome

    Sequencing analysis of the MYCN gene.

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  3. Noonan Syndrome

    Sequencing analysis of exons 3, 8, 9, 13 of the PTPN11 gene

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  4. Chondrodysplasia

    Sequencing analysis of the RUNX2gene

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  5. Robinow Syndrome

    Sequencing analysis of the ROR2 gene

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  6. Achondroplasia (ACH)

    Sequencing analysis of the most common mutations G380R and G375C in the FGFR3 gene.

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  7. Hypochondroplasia (HCH),analysis of thr 6 the most common mutations in the FGFR3 gene

    Sequencing analysis of the most common mutations in the FGFR3 gene (fibroblast growth factor…

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