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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

A Türkyılmaz

A Türkyılmaz

Department of Medical Genetics, Erzurum Region Training and Research Hospital, Department of Medical GeneticsErzurum, Turkey
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Türkyılmaz, A
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O Yaralı

O Yaralı

Department of Medical Genetics, Erzurum Region Training and Research Hospital, Department of Medical GeneticsErzurum, Turkey
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Yaralı, O
  
Aug 26, 2020
A very rare partial trisomy syndrome: De novo duplication of 16q12.1q23.3 in a Turkish girl with developmental delay and facial dysmorphic features's Cover Image
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Article Category: Case Report
Published Online: Aug 26, 2020
Page range: 103 - 108
DOI: https://doi.org/10.2478/bjmg-2020-0009
Keywords
© 2020 Türkyılmaz A, Yaralı O, published by Sciendo
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.
Language:
English
Publication timeframe:
2 times per year
Journal Subjects:
Medicine, Basic Medical Science, Basic Medical Science, other
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