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

• 主要な著者: Zhao Linlu (著者), Triche Elizabeth W (著者), Walsh Kyle M (著者), Bracken Michael B (著者), Saftlas Audrey F (著者), Hoh Josephine (著者), Dewan Andrew T (著者)
• フォーマット: 図書
• 出版事項: BMC, 2012-06-01T00:00:00Z.
• 主題: article
• オンライン･アクセス: Connect to this object online.

<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...