Detection of copy number variants with chromosomal microarray in 10 377 pregnancies at a single laboratory

INTRODUCTION: Invasive prenatal testing with chromosomal microarray analysis may be a relevant option for all pregnant women, but there is only moderate‐quality evidence for such an offer. We intended to study the prevalence of copy number variants (CNVs) in prenatal samples using a single SNP‐array...

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Detalles Bibliográficos
Autores principales: Lin, Yi‐Hui, Jong, Yiin‐Jeng, Huang, Pin‐Chia, Tsai, Chris
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Whole Genome Based Methods: Chromosomal Microarray and Whole Exome Sequencing
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7383919/
https://www.ncbi.nlm.nih.gov/pubmed/32346853
http://dx.doi.org/10.1111/aogs.13886

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7383919/
https://www.ncbi.nlm.nih.gov/pubmed/32346853
http://dx.doi.org/10.1111/aogs.13886

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