Preserved Fertility in a Patient with a 46,XY Disorder of Sex Development due to a New Heterozygous Mutation in the NR5A1/SF-1 Gene: Evidence of 46,XY and 46,XX Gonadal Dysgenesis Phenotype Variability in Multiple Members of an Affected Kindred

Publisher： Karger

E-ISSN： 1663-2826|78|2|119-126

ISSN： 1663-2818

Source： Hormone Research in Paediatrics, Vol.78, Iss.2, 2012-08, pp. : 119-126

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