Genome-wide association study identifies a maternal copy-number deletion in PSG11 enriched among preeclampsia patients

BACKGROUND: Specific genetic contributions for preeclampsia (PE) are currently unknown. This genome-wide association study (GWAS) aims to identify maternal single nucleotide polymorphisms (SNPs) and copy-number variants (CNVs) involved in the etiology of PE. METHODS: A genome-wide scan was performed...

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Bibliografiske detaljer
Main Authors: Zhao, Linlu, Triche, Elizabeth W, Walsh, Kyle M, Bracken, Michael B, Saftlas, Audrey F, Hoh, Josephine, Dewan, Andrew T
Format: Artigo
Sprog:Inglês
Udgivet: BioMed Central 2012
Fag:
Research Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3476390/
https://ncbi.nlm.nih.gov/pubmed/22748001
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2393-12-61
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