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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Main Authors: Zhao Linlu (Author), Triche Elizabeth W (Author), Walsh Kyle M (Author), Bracken Michael B (Author), Saftlas Audrey F (Author), Hoh Josephine (Author), Dewan Andrew T (Author)
Format: Book
Published: BMC, 2012-06-01T00:00:00Z.
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