Figure 1
Parietal cephalocele of the affacted individual.
Figure 2
The aCGH showing the loss of 18p11.32-p11.31 (A) and gain of 6q25-27 (B) resulting from the de novo unbalanced translocation in the affected individual.
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
DOI: https://doi.org/10.2478/bjmg-2020-0014 | Journal eISSN: 2199-5761 (formerly 1311-0160) | Journal ISSN: 1311-0160
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
Keywords:
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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.