Chromosomal microarray analysis for prenatal diagnosis of uniparental disomy: a retrospective study

Abstract Background Chromosomal microarray analysis (CMA) is a valuable tool in prenatal diagnosis for the detection of chromosome uniparental disomy (UPD). This retrospective study examines fetuses undergoing invasive prenatal diagnosis through Affymetrix CytoScan 750 K array analysis. We evaluated...

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Bibliografiset tiedot

Päätekijät:	Chenxia Xu, Miaoyuan Li, Tiancai Gu, Fenghua Xie, Yanfang Zhang, Degang Wang, Jianming Peng
Aineistotyyppi:	Artigo
Kieli:	Inglês
Julkaistu:	BMC 2024-01-01
Sarja:	Molecular Cytogenetics
Aiheet:	Chromosomal microarray Prenatal diagnosis Regions of homozygosity SNP arrays Uniparental disomy
Linkit:	https://doi.org/10.1186/s13039-023-00668-8
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