Prenatal diagnosis of 7 cases with uniparental disomy by utilization of single nucleotide polymorphism array

Prenatal diagnosis of 7 cases with uniparental disomy by utilization of single nucleotide polymorphism array

Abstract Background The phenotypes of uniparental disomy (UPD) are variable, which may either have no clinical impact, lead to clinical signs and symptoms. Molecular analysis is essential for making a correct diagnosis. This study involved a retrospective analysis of 4512 prenatal diagnosis samples...

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Bibliographic Details
Main Authors: Lili Zhou, Zhaoke Zheng, Yunzhi Xu, Xiaoxiao Lv, Chenyang Xu, Xueqin Xu
Format: Article
Language:English
Published: BMC 2021-03-01
Series:Molecular Cytogenetics
Subjects:
uniparental disomy
single nucleotide polymorphism array
prenatal diagnosis
Online Access:https://doi.org/10.1186/s13039-021-00537-2

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