A case of prenatal diagnosis of 18p deletion syndrome following noninvasive prenatal testing

A case of prenatal diagnosis of 18p deletion syndrome following noninvasive prenatal testing

Abstract Background Chromosome 18p deletion syndrome is a disease caused by the complete or partial deletion of the short arm of chromosome 18, there were few cases reported about the prenatal diagnosis of 18p deletion syndrome. Noninvasive prenatal testing (NIPT) is widely used in the screening of...

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Bibliographic Details
Main Authors: Ganye Zhao, Peng Dai, Shanshan Gao, Xuechao Zhao, Conghui Wang, Lina Liu, Xiangdong Kong
Format: Article
Language:English
Published: BMC 2019-12-01
Series:Molecular Cytogenetics
Subjects:
NIPT
18p deletion syndrome
Karyotype
CNV-seq
Prenatal diagnosis
Online Access:https://doi.org/10.1186/s13039-019-0464-y

Internet

https://doi.org/10.1186/s13039-019-0464-y

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