Prenatal diagnosis of a de novo partial trisomy 6q and partial monosomy 18p associated with cephalocele: A case report
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Aug 26, 2020
About this article
Article Category: Case Report
Published Online: Aug 26, 2020
Page range: 99 - 102
DOI: https://doi.org/10.2478/bjmg-2020-0014
Keywords
© 2020 Karaman A, Karaman B, Çetinkaya A, Karaman S, Demirci O, published by Sciendo
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.
Karaman, A
Genetics Diagnosis Center, University of Health Sciences, Zeynep Kamil Women and Children Training and Research HospitalIstanbul, Turkey
Karaman, B
Department of Medical Genetics, Istanbul University, Istanbul Faculty of MedicineIstanbul, Turkey
Çetinkaya, A
Genetics Diagnosis Center, University of Health Sciences, Zeynep Kamil Women and Children Training and Research HospitalIstanbul, Turkey
Department of Medical Genetics, Hacetepe University, Faculty of MedicineAnkara, Turkey
Karaman, S
Department of Anesthesia and Reanimation, University of Health Sciences Ümraniye Training and Research HospitalIstanbul, Turkey
Demirci, O
Perinatalogy Unit, University of Health Sciences Zeynep Kamil Women and Children Training and Research HospitalIstanbul, Turkey