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
Mónica Fernández-Cancio, Emilio García-García, Carmen González-Cejudo, María Angeles Martínez-Maestre, Miguel Angel Mangas-Cruz, Gil Guerra-Junior, Maricilda Pandi De Mello, Ivo J.P. Arnhold, Mirian Y. Nishi, Berenice Bilharinho Mendonça, Elena García-Arumí, Laura Audí, Eduardo Tizzano, Antonio Carrascosa
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