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

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

<p>Abstract</p> <p>Background</p> <p>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 et...

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Bibliographic Details
Main Authors: Zhao Linlu, Triche Elizabeth W, Walsh Kyle M, Bracken Michael B, Saftlas Audrey F, Hoh Josephine, Dewan Andrew T
Format: Article
Language:English
Published: BMC 2012-06-01
Series:BMC Pregnancy and Childbirth
Subjects:
Copy-number variant
Genome-wide association study
Microarray analysis
Preeclampsia
Single nucleotide polymorphism
Online Access:http://www.biomedcentral.com/1471-2393/12/61

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http://www.biomedcentral.com/1471-2393/12/61

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