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
Authors
V Tasic
Medical Faculty Skopje, Skopje, Republic of Macedonia
A Mitrotti
Division of Nephrology, Columbia University, New York, NY, USA
FG Riepe
Division of Pediatric Endocrinology and Diabetes, Department of Pediatrics, University Hospital Schleswig-Holstein, Christian-Albrechts University Kiel, Kiel, Germany
AE Kulle
Division of Pediatric Endocrinology and Diabetes, Department of Pediatrics, University Hospital Schleswig-Holstein, Christian-Albrechts University Kiel, Kiel, Germany
N Laban
Medical Faculty Skopje, Skopje, Republic of Macedonia
M Polenakovic
Research Centre for Genetic Engineering and Biotechnology "Georgi D. Efremov," Macedonian Academy of Sciences and Arts, Skopje, Republic of Macedonia
D Plaseska-Karanfilska
Research Centre for Genetic Engineering and Biotechnology "Georgi D. Efremov," Macedonian Academy of Sciences and Arts, Skopje, Republic of Macedonia
S Sanna-Cherchi
Division of Nephrology, Columbia University, New York, NY, USA
M Kostovski
Medical Faculty Skopje, Skopje, Republic of Macedonia
DOI: https://doi.org/10.2478/bjmg-2019-0006 | Journal eISSN: 2199-5761
Language: English
Page range: 81 - 88
Published on: Aug 28, 2019
Published by: Macedonian Academy of Sciences and Arts
In partnership with: Paradigm Publishing Services
Publication frequency: 2 issues per year
Keywords:
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© 2019 V Tasic, A Mitrotti, FG Riepe, AE Kulle, N Laban, M Polenakovic, D Plaseska-Karanfilska, S Sanna-Cherchi, M Kostovski, Z Gucev, published by Macedonian Academy of Sciences and Arts
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.