Prenatal diagnosis of a de novo partial trisomy 6q and partial monosomy 18p associated with cephalocele: A case report
By: A Karaman, B Karaman, A Çetinkaya, S Karaman and O Demirci
Authors
A Karaman
Genetics Diagnosis Center, University of Health Sciences, Zeynep Kamil Women and Children Training and Research Hospital, Istanbul, Turkey
B Karaman
Department of Medical Genetics, Istanbul University, Istanbul Faculty of Medicine, Istanbul, Turkey
A Çetinkaya
Genetics Diagnosis Center, University of Health Sciences, Zeynep Kamil Women and Children Training and Research Hospital, Istanbul, Turkey
Department of Medical Genetics, Hacetepe University, Faculty of Medicine, Ankara, Turkey
S Karaman
Department of Anesthesia and Reanimation, University of Health Sciences Ümraniye Training and Research Hospital, Istanbul, Turkey
O Demirci
Perinatalogy Unit, University of Health Sciences Zeynep Kamil Women and Children Training and Research Hospital, Istanbul, Turkey
Language: English
Page range: 99 - 102
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 Karaman, B Karaman, A Çetinkaya, S Karaman, O Demirci, published by Macedonian Academy of Sciences and Arts
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.