Double isochromosome X, A rare cytogenetic variant of turner syndrome: A case report and a review of the literature
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Authors
K. Zerrouki
Faculty of Medicine and Pharmacy, Mohammed Premier University, Oujda, Morocco
Medical Genetics Laboratory, Mohammed VI University Hospital, Oujda, Morocco
A. Babakhouya
Faculty of Medicine and Pharmacy, Mohammed Premier University, Oujda, Morocco
Pediatrics department, Mother and Child Hospital, Mohammed VI University Hospital, Oujda, Morocco
M. Tajir
Faculty of Medicine and Pharmacy, Mohammed Premier University, Oujda, Morocco
Medical Genetics Laboratory, Mohammed VI University Hospital, Oujda, Morocco
DOI: https://doi.org/10.2478/bjmg-2022-0011 | Journal eISSN: 2199-5761
Language: English
Page range: 101 - 104
Published on: Mar 1, 2023
Published by: Macedonian Academy of Sciences and Arts
In partnership with: Paradigm Publishing Services
Publication frequency: 2 issues per year
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© 2023 K. Zerrouki, A. Babakhouya, M. Tajir, published by Macedonian Academy of Sciences and Arts
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.