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

Research output: Contribution to journalArticleResearchpeer-review

3 Citations (Scopus)

Fingerprint Dive into the research topics of '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'. Together they form a unique fingerprint.

Medicine & Life Sciences