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A very rare partial trisomy syndrome: De novo duplication of 16q12.1q23.3 in a Turkish girl with developmental delay and facial dysmorphic features Cover

A very rare partial trisomy syndrome: De novo duplication of 16q12.1q23.3 in a Turkish girl with developmental delay and facial dysmorphic features

Balkan Journal of Medical Genetics
Volume 23 (2020): Issue 1 (June 2020)
By: A Türkyılmaz and  O Yaralı  
Open Access
|Aug 2020

Authors

A Türkyılmaz

ayberkturkyilmaz@gmail.com

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
DOI: https://doi.org/10.2478/bjmg-2020-0009 | Journal eISSN: 2199-5761
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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
Keywords:
Array comparative genomic hybridization (aCGH),
Partial trisomy 16,
16q duplication
Related subjects:
Medicine,
Basic medical science,
Basic medical science, other

© 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.

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