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A report on seven fetal cases associated with 15q11-q13 microdeletion and microduplication.

Molecular genetics & genomic medicine - 1 Mar 2021

Huang Xiuzhu, Chen Jieping, Hu Wenlong, Li Lu, He Huiyan, Guo Hui, Liao Qiuyan, Ye Mei, Tang Donge, Dai Yong

Abstract excerpt

BACKGROUND: The 15q11-q13 region contains three breakpoints (BP1 to BP3), and copy number variations often occur in the region. AIMS: 15q11-q13 microdeletion and microduplication are usually associated with Prader-Willi and Angelman syndromes, respectively. It is not yet clear to what extent microdeletion and microduplication affect the physical health of the fetus and the child. In this study, we examined seven...

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Amniocentesis
Chromosome Aberrations
Chromosomes, Human, Pair 15
Fetus
Genetic Testing

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PMID: 33538077
DOI: 10.1002/mgg3.1605
PMCID: PMC8104164

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