Molecular analysis of exons 8, 9 and 10 of the fibroblast growth factor receptor 2 (FGFR2) gene in two families with index cases of Apert Syndrome

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Bibliographic Details
Main Author:	Lilian Torres
Format:	Artículo científico
Language:	en
Published:	Universidad del Valle 2015
Subjects:	Medicina intron mutation FGFR2 gene cleft palate Apert syndrome
Online Access:	Acceder al recurso 1 Acceder al recurso 2 Acceder al recurso 3 Acceder al recurso 4 Acceder al recurso 5
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