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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

✍ Scribed by Ciaccio, Marta; Costanzo, Mariana; Guercio, Gabriela; De Dona, Valeria; Marino, Roxana; Ramirez, Pablo C.; Galeano, Jessica; Warman, Diana Monica; Berensztein, Esperanza; Saraco, Nora; Baquedano, Maria Sonia; Chaler, Eduardo; Maceiras, Mercedes; Lazzatti, Juan Manuel; Rivarola, Marco A.; Belgorosky, Alicia

Book ID: 118747715
Publisher: S. Karger AG
Year: 2012
Tongue: English
Weight: 415 KB
Volume: 78
Category: Article
ISSN: 1663-2818
DOI: 10.1159/000338346

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