Phenotypic Variability of 17q12 Microdeletion Syndrome – Three Cases and Review of Literature
By: A Țuțulan-Cuniță, AG Pavel, L Dimos, M Nedelea, A Ursuleanu, AT Neacșu, M Budișteanu and D Stambouli
Authors
AG Pavel
Cytogenomic Medical Laboratory, Bucharest, Romania
L Dimos
Cytogenomic Medical Laboratory, Bucharest, Romania
M Nedelea
Cytogenomic Medical Laboratory, Bucharest, Romania
Medical Genetics Department, Carol Davila University of Medicine, Bucharest, Romania
Medical Genetics Department, Filantropia Clinical Hospital, Bucharest, Romania
A Ursuleanu
Obstetrics & Gynecology Clinic, Prof. Dr. Ioan Cantacuzino Clinical Hospital, Bucharest, Romania
AT Neacșu
Cytogenomic Medical Laboratory, Bucharest, Romania
M Budișteanu
Pediatric Neurology Clinic, Prof. Dr. Alex. Obregia Clinical Hospital of Psychiatry, Bucharest, Romania
Medical Genetics Laboratory, Victor Babes National Institute of Pathology, Bucharest, Romania
Faculty of Medicine, Titu Maiorescu University, Bucharest, Romania
D Stambouli
Cytogenomic Medical Laboratory, Bucharest, Romania
DOI: https://doi.org/10.2478/bjmg-2021-0025 | Journal eISSN: 2199-5761
Language: English
Page range: 71 - 82
Published on: Jun 5, 2022
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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© 2022 A Țuțulan-Cuniță, AG Pavel, L Dimos, M Nedelea, A Ursuleanu, AT Neacșu, M Budișteanu, D Stambouli, published by Macedonian Academy of Sciences and Arts
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.