Prenatal diagnosis of fetuses with 15q11.2 BP1-BP2 microdeletion in the Chinese population: a seven-year single-center retrospective study

Prenatal diagnosis of fetuses with 15q11.2 BP1-BP2 microdeletion in the Chinese population: a seven-year single-center retrospective study

Abstract Background The 15q11.2 BP1-BP2 microdeletion syndrome is associated with developmental delays, language impairments, neurobehavioral disorders, and psychiatric complications. The aim of the present study was to provide prenatal and postnatal clinical data for 16 additional fetuses diagnosed...

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Bibliographic Details
Main Authors: Jianlong Zhuang, Na Zhang, Wanyu Fu, Yuying Jiang, Yu’e Chen, Chunnuan Chen
Format: Article
Language:English
Published: BMC 2024-09-01
Series:Molecular Cytogenetics
Subjects:
15q11.2 BP1-BP2 microdeletion
Chromosomal microarray analysis
Karyotype analysis
Prenatal diagnosis
Whole exome sequencing
Online Access:https://doi.org/10.1186/s13039-024-00690-4

Internet

https://doi.org/10.1186/s13039-024-00690-4

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