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.

Published in:

Sexual Development, 2017, v. 11, n. 2, p. 70, doi. 10.1159/000468160

By:

• Fernández-Cancio, Mónica;
• García-García, Emilio;
• González-Cejudo, Carmen;
• Martínez-Maestre, María-angeles;
• Mangas-Cruz, Miguel-angel;
• Guerra-Junior, Gil;
• Pandi de Mello, Maricilda;
• arnhold, Ivo J.P.;
• Nishi, Mirian Y.;
• Bilharinho Mendonça, Berenice;
• García-arumí, Elena;
• audí, Laura;
• Tizzano, Eduardo;
• Carrascosa, antonio

Publication type:

Article