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
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28 août 2019
À propos de cet article
Catégorie d'article: Case Report
Publié en ligne: 28 août 2019
Pages: 81 - 88
DOI: https://doi.org/10.2478/bjmg-2019-0006
Mots clés
© 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.
Tasic, V
Medical Faculty SkopjeSkopje, Republic of Macedonia
Mitrotti, A
Division of Nephrology, Columbia UniversityNew York, NY, USA
Riepe, FG
Division of Pediatric Endocrinology and Diabetes, Department of Pediatrics, University Hospital Schleswig-Holstein, Christian-Albrechts University KielKiel, Germany
Kulle, AE
Division of Pediatric Endocrinology and Diabetes, Department of Pediatrics, University Hospital Schleswig-Holstein, Christian-Albrechts University KielKiel, Germany
Laban, N
Medical Faculty SkopjeSkopje, Republic of Macedonia
Polenakovic, M
Research Centre for Genetic Engineering and Biotechnology "Georgi D. Efremov," Macedonian Academy of Sciences and ArtsSkopje, Republic of Macedonia
Plaseska-Karanfilska, D
Research Centre for Genetic Engineering and Biotechnology "Georgi D. Efremov," Macedonian Academy of Sciences and ArtsSkopje, Republic of Macedonia
Sanna-Cherchi, S
Division of Nephrology, Columbia UniversityNew York, NY, USA
Kostovski, M
Medical Faculty SkopjeSkopje, Republic of Macedonia
Gucev, Z
Medical Faculty SkopjeSkopje, Republic of Macedonia