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...
Main Authors: | , , , , , , |
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Format: | Article |
Language: | English |
Published: |
BMC
2012-06-01
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Series: | BMC Pregnancy and Childbirth |
Subjects: | |
Online Access: | http://www.biomedcentral.com/1471-2393/12/61 |