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Prenatal diagnosis of a de novo partial trisomy 6q and partial monosomy 18p associated with cephalocele: A case report Cover

Prenatal diagnosis of a de novo partial trisomy 6q and partial monosomy 18p associated with cephalocele: A case report

Balkan Journal of Medical Genetics
Volume 23 (2020): Issue 1 (June 2020)
By: A Karaman,  B Karaman,  A Çetinkaya,  S Karaman and  O Demirci  
Open Access
|Aug 2020

Figures & Tables

Figure 1

Parietal cephalocele of the affacted individual.
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.
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.
DOI: https://doi.org/10.2478/bjmg-2020-0014 | Journal eISSN: 2199-5761
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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
Keywords:
18p Monosomy,
Prenatal diagnosis,
6q Trisomy
Related subjects:
Medicine,
Basic medical science,
Basic medical science, other

© 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.

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