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Genetic correlation between fetal nuchal translucency thickening and cystic hygroma and exploration of pregnancy outcome

Abstract Chromosome microarray analysis (CMA) and whole exome sequencing (WES) are increasingly utilized in prenatal diagnosis of abnormal ultrasound findings, but studies on correlation between pathogenic copy number variations (pCNVs) and single-gene mutations in fetuses with nuchal translucency (...

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Kaydedildi:
Asıl Yazarlar: Jianli Zheng, Tiantian Wang, Huilin Sun, Yongjuan Guan, Fangfang Yang, Jing Wu, Feifei Ying, Yadong Fu, Min Li, Jianbing Liu
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Nature Portfolio 2024-11-01
Seri Bilgileri:Scientific Reports
Konular:
Nuchal translucency thickening
Nuchal cystic hygroma
Genetic examination
Prenatal diagnosis
Follow-up
Online Erişim:https://doi.org/10.1038/s41598-024-76628-y
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