sindrome di Apert

Also known as type I acrocephalosyndactyly

malattia

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Image: Patient with Apert syndrome.jpg

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Article · Italiano

La sindrome di Apert o acrocefalosindattilia ereditaria è un disordine congenito raro a carattere ereditario autosomico dominante e . Mutazione Cys755Gly in eterozigosi. Cromosoma 10q26.

Abstract from DBpedia / Wikipedia · CC BY-SA

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sindrome di Apert

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Article · Italiano

Available in 21 languages

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