File:Hands in Apert syndrome.jpg

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Syndactyly in Apert syndrome. Clinical picture of premature closure of cranial sutures, syndactyly on the legs and hands. Cause of mutation of the FGFR2 gene (AD) in the region 10q26.13

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current21:15, 15 March 2023Thumbnail for version as of 21:15, 15 March 2023225 × 177 (12 KB)Sam02 (talk | contribs)

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