A very rare partial trisomy syndrome: De novo duplication of 16q12.1q23.3 in a Turkish girl with developmental delay and facial dysmorphic features
By: A Türkyılmaz and O Yaralı
Authors
A Türkyılmaz
Department of Medical Genetics, Erzurum Region Training and Research Hospital, Department of Medical Genetics, Erzurum, Turkey
O Yaralı
Department of Medical Genetics, Erzurum Region Training and Research Hospital, Department of Medical Genetics, Erzurum, Turkey
Language: English
Page range: 103 - 108
Published on: Aug 26, 2020
Published by: Macedonian Academy of Sciences and Arts
In partnership with: Paradigm Publishing Services
Publication frequency: 2 issues per year
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© 2020 A Türkyılmaz, O Yaralı, published by Macedonian Academy of Sciences and Arts
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.