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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...
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 |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
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 |
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