Duplication of the SOX3 gene in an sry-negative 46,XX male with associated congenital anomalies of kidneys and the urinary tract: Case report and review of the literature

Kategoria artykułu: Case Report

Data publikacji: 28 sie 2019

Zakres stron: 81 - 88

DOI: https://doi.org/10.2478/bjmg-2019-0006

Słowa kluczowe

Congenital anomalies of kidneys and the urinary tract (CAKUT), Copy number variations (CNVs), Disorders of sex development (DSD)

© 2019 Tasic V, Mitrotti A, Riepe FG, Kulle AE, Laban N, Polenakovic M, Plaseska-Karanfilska D, Sanna-Cherchi S, Kostovski M, Gucev Z, published by Sciendo

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.