Intrauterine ultrasound phenotyping, molecular characteristics, and postnatal follow-up of fetuses with the 15q11.2 BP1-BP2 microdeletion syndrome: a single-center, retrospective clinical study

Intrauterine ultrasound phenotyping, molecular characteristics, and postnatal follow-up of fetuses with the 15q11.2 BP1-BP2 microdeletion syndrome: a single-center, retrospective clinical study

Abstract Objectives The 15q11.2 BP1-BP2 microdeletion is associated with neurodevelopmental diseases. However, most studies on this microdeletion have focused on adults and children. Thus, in this study, we summarized the molecular characteristics of fetuses with the 15q11.2 BP1-BP2 microdeletion an...

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Bibliographic Details
Main Authors: Meiying Cai, Aixiang Lv, Wantong Zhao, Liangpu Xu, Na Lin, Hailong Huang
Format: Article
Language:English
Published: BMC 2024-01-01
Series:BMC Pregnancy and Childbirth
Subjects:
15q11.2 BP1-BP2 microdeletion syndrome
Prenatal phenotyping
Postnatal follow-up
Mental retardation
Copy number variation
Online Access:https://doi.org/10.1186/s12884-023-06223-y

Internet

https://doi.org/10.1186/s12884-023-06223-y

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