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The use of high-resolution SNP arrays to detect congenital cardiac defects.

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 - 1 Dec 2024

Linhuan Huang, Danlei Cai, Zhiming He, Shu Kong, Jiayi Chen, Jiayi Peng, Chuqi Su, Yinghong Yang, Ding Wang, Yingjun Xie, Yanmin Luo

Abstract excerpt

OBJECTIVE: Copy number variations (CNVs) detected by high-resolution single nucleotide polymorphism microarrays (SNP arrays) have been associated with congenital heart defects (CHDs). The genetic mechanism underlying the development of CHDs remains unclear. METHODS: High-resolution SNP arrays were used to detect CNVs and traditional chromosomal analyses, respectively, were carried out on 60 and 249 fetuses from...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 38311547
DOI: 10.1080/14767058.2024.2301831

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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