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

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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Detalhes bibliográficos
Principais autores: Chenxia Xu, Miaoyuan Li, Tiancai Gu, Fenghua Xie, Yanfang Zhang, Degang Wang, Jianming Peng
Formato: Artigo
Idioma:English
Publicado em: BMC 2024-01-01
coleção:Molecular Cytogenetics
Assuntos:
Chromosomal microarray
Prenatal diagnosis
Regions of homozygosity
SNP arrays
Uniparental disomy
Acesso em linha:https://doi.org/10.1186/s13039-023-00668-8

Internet

https://doi.org/10.1186/s13039-023-00668-8

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