Discordant Genotypic Sex and Phenotype Variations in Two Spanish Siblings with 17α-Hydroxylase/17,20-Lyase Deficiency Carrying the Most Prevalent Mutated CYP17A1 Alleles of Brazilian Patients

Publisher: Karger

E-ISSN: 1661-5433|11|2|70-77

ISSN: 1661-5425

Source: Sexual Development, Vol.11, Iss.2, 2017-04, pp. : 70-77

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Abstract