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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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| Publicat a: | J Clin Lab Anal |
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| Autors principals: | , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
John Wiley and Sons Inc.
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7439336/ https://ncbi.nlm.nih.gov/pubmed/32342531 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jcla.23347 |
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