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7 févr. 1894 - Apert syndrome - acrocephalosyndactyly I

Description:

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.

Ajouté au bande de temps:

24 oct. 2017
0
0
444

Date:

7 févr. 1894
Maintenaint
~ Il y a 131 ans