Showing results for: FGFR2   Total: 3

  1. Pfeiffer Syndrome

    Sequencing analysis of the FGFR2 gene (two exons with common mutations)

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  2. APERT-CROUZON DISEASE

    Sequencing analysis of the FGFR2 (e3a, e3c) gene - 2 common mutations p.S252W i p.P253R

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  3. Crouzon Syndrome

    Sequencing analysis of the FGFR2 gene (3a and 3c exons).

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