Fetus of 8q22.2q24.3 duplication and 13q33.2q34 deletion derived from a maternal balanced translocation
Author:
Affiliation:
1. Department of Prenatal Diagnosis Medical Center, XuZhou Central HospitalXuZhou Clinical School of Xuzhou Medical University Jiangsu China
Funder
Wu Jieping Medical Foundation
Publisher
Wiley
Subject
Obstetrics and Gynecology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/jog.14386
Reference22 articles.
1. Detection of fetal copy number variants by non-invasive prenatal testing for common aneuploidies
2. Limited Clinical Utility of Non-invasive Prenatal Testing for Subchromosomal Abnormalities
3. A foetus with 18p11.32-q21.2 duplication and Xp22.33-p11.1 deletion derived from a maternal reciprocal translocation t(X;18)(q13;q21.3)
4. 10p15.3p13 duplication inherited from paternal balance translocation (46,XY,t(5;10)(q35.1;p13)) identified on non-invasive prenatal testing
5. Noninvasive prenatal testing for fetal subchromosomal copy number variations and chromosomal aneuploidy by low‐pass whole‐genome sequencing;Yu DY;Mol Genet Genomic Med,2019
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1. Prenatal Diagnosis of Complex Copy Number Variants in the Fetus and Associated Cytogenetic Findings in Parents;Clinical and Experimental Obstetrics & Gynecology;2023-10-18
2. Wolf-Hirschhorn syndrome with intrauterine growth restriction in a fetus: A case report;Medicine: Case Reports and Study Protocols;2022-09-01
3. Noninvasive prenatal testing: How far can we reach detecting fetal copy number variations;European Journal of Obstetrics & Gynecology and Reproductive Biology;2022-05
4. Inherited unbalanced reciprocal translocation with 3q duplication and 5p deletion in a foetus revealed by cell-free foetal DNA (cffDNA) testing: a case report;European Journal of Medical Research;2021-06-29
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