Homozygous Mutation of the FGFR1 Gene Associated with Congenital Heart Disease and 46,XY Disorder of Sex Development

Publisher: Karger

E-ISSN: 1661-5433|10|1|16-22

ISSN: 1661-5425

Source: Sexual Development, Vol.10, Iss.1, 2016-04, pp. : 16-22

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Abstract