鼻骨
核型
三体
胎儿
产前诊断
非整倍体
医学
单体
生物
染色体
病理
遗传学
解剖
怀孕
基因
作者
Xinying Chen,Yuying Jiang,Shuhong Zeng,Jianlong Zhuang,Na Lin
出处
期刊:Teratology
[Wiley]
日期:2024-05-01
卷期号:116 (5)
摘要
Pathogenic copy number variants (pCNVs) are associated with fetal ultrasound anomalies, which can be efficiently identified through chromosomal microarray analysis (CMA). The primary objective of the present study was to enhance understanding of the genotype-phenotype correlation in fetuses exhibiting absent or hypoplastic nasal bones using CMA.
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