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Updated: Jul 4, 2025

Fetal Mouse Cardiovascular Imaging Using a High-frequency Ultrasound 30/45MHZ System
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使用高分辨率SNP阵列来检测先天性心脏缺陷

Huang Linhuan1, Cai Danlei2, He Zhiming1

  • 1Department of Obstetrics and Gynecology, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou, People's Republic of China.

The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians
|February 4, 2024
PubMed
概括

高分辨率SNP阵列有效检测具有先天性心脏缺陷 (CHD) 的胎儿的副本数变异 (CNV),提高诊断率和澄清遗传原因.

关键词:
染色体微阵列分析遗传性心脏缺陷 遗传性心脏缺陷副本编号变化 副本编号变化在产前诊断 产前诊断单个核酸多态化微阵列

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相关概念视频

Genome-wide Association Studies-GWAS01:11

Genome-wide Association Studies-GWAS

Genome-wide association studies or GWAS are used to identify whether common SNPs are associated with certain diseases. Suppose specific SNPs are more frequently observed in individuals with a particular disease than those without the disease. In that case, those SNPs are said to be associated with the disease. Chi-square analysis is performed to check the probability of the allele likely to be associated with the disease.
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