Analysis of copy number variation by sequencing in fetuses with nuchal translucency thickening

OBJECTIVE: Copy number variation sequencing (CNV‐seq) technique was used to analyze the genetic etiology of fetuses with increased nuchal translucency (NT). METHODS: A total of 139 women with gestational 11‐14 weeks whose fetuses were detected with increased NT (NT ≥ 2.5 mm) in our hospital from Jul...

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Detalles Bibliográficos
Autores principales: Lan, Liubing, Wu, Heming, She, Lingna, Zhang, Bosen, He, Yanhong, Luo, Dandan, Wang, Huaxian, Zheng, Zhiyuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7439336/
https://www.ncbi.nlm.nih.gov/pubmed/32342531
http://dx.doi.org/10.1002/jcla.23347

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7439336/
https://www.ncbi.nlm.nih.gov/pubmed/32342531
http://dx.doi.org/10.1002/jcla.23347

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