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Phenotypic Variability of 17q12 Microdeletion Syndrome – Three Cases and Review of Literature

Open Access
|Jun 2022

Authors

A Țuțulan-Cuniță

cunita@cytogenomic.ro

Cytogenomic Medical Laboratory, Bucharest, Romania

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
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

© 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.