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7 Feb 1894 Jahr - Apert syndrome - acrocephalosyndactyly I

Beschreibung:

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.

Zugefügt zum Band der Zeit:

medicine curiosity

ByMoises Littig
24 Okt 2017
0
0
445

Datum:

7 Feb 1894 Jahr
Jetzt
~ 131 years ago
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