Works matching IS 16615425 AND DT 2017 AND VI 11 AND IP 2


Results: 7
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    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
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