Mutation c.943G>T (p.Ala315Ser) in FGFR2 Causing a Mild Phenotype of Crouzon Craniofacial Dysostosis in a Three-Generation Family

Publisher: Karger

E-ISSN: 1661-8777|8|2|93-97

ISSN: 1661-8769

Source: Molecular Syndromology, Vol.8, Iss.2, 2017-01, pp. : 93-97

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Abstract