The Prenatal Diagnosis and Clinical Outcomes of Fetuses With 15q11.2 Copy Number Variants: A Case Series of 36 Patients

The Prenatal Diagnosis and Clinical Outcomes of Fetuses With 15q11.2 Copy Number Variants: A Case Series of 36 Patients

Prenatal genetic counseling of fetuses diagnosed with 15q11.2 copy number variants (CNVs) involving the BP1–BP2 region is difficult due to limited information and controversial opinion on prognosis. In total, we collected the data of 36 pregnant women who underwent prenatal microarray analysis from...

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Autores principales: Jessica Kang, Chien-Nan Lee, Yi-Ning Su, Ming-Wei Lin, Yi-Yun Tai, Wen-Wei Hsu, Kuan-Ying Huang, Chi-Ling Chen, Chien-Hui Hung, Shin-Yu Lin
Formato: article
Lenguaje:EN
Publicado: Frontiers Media S.A. 2021
Materias:
15q11.2 microdeletion
15q11.2 microduplication
BP1–BP2
copy number variant
chromosome microarray analysis (CMA)
prenatal
Medicine (General)
R5-920
Acceso en línea:https://doaj.org/article/42dd194fdf3c469b89233c20679cb7c2
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https://doaj.org/article/42dd194fdf3c469b89233c20679cb7c2

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