Double isochromosome X, A rare cytogenetic variant of turner syndrome: A case report and a review of the literature
By: K. Zerrouki, A. Babakhouya and M. Tajir
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 (formerly 1311-0160) | Journal ISSN: 1311-0160
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
Keywords:
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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.