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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Detalles Bibliográficos
Autores principales: Kang, Jessica, Lee, Chien-Nan, Su, Yi-Ning, Lin, Ming-Wei, Tai, Yi-Yun, Hsu, Wen-Wei, Huang, Kuan-Ying, Chen, Chi-Ling, Hung, Chien-Hui, Lin, Shin-Yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8649837/
https://www.ncbi.nlm.nih.gov/pubmed/34888324
http://dx.doi.org/10.3389/fmed.2021.754521

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8649837/
https://www.ncbi.nlm.nih.gov/pubmed/34888324
http://dx.doi.org/10.3389/fmed.2021.754521

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