7 feb 1894 anni - Apert syndrome - acrocephalosyndactyly I
Descrizione:
It is named after Eugene Apert, French physician, in 1906 although some reports suggest it was first described by Wheaton
defect on the fibroblast growth factor receptor 2 (FGFR2) gene, located on chromosome 10q26.
Aggiunto al nastro di tempo:
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