Your browser doesn't support javascript.
loading
Genome-wide association study identifies a maternal copy-number deletion in PSG11 enriched among preeclampsia patients.
Zhao, Linlu; Triche, Elizabeth W; Walsh, Kyle M; Bracken, Michael B; Saftlas, Audrey F; Hoh, Josephine; Dewan, Andrew T.
Affiliation
  • Zhao L; Center for Perinatal, Pediatric and Environmental Epidemiology, Yale School of Public Health, New Haven, CT 06520, USA.
BMC Pregnancy Childbirth ; 12: 61, 2012 Jun 29.
Article in En | MEDLINE | ID: mdl-22748001

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pre-Eclampsia / Pregnancy-Specific beta 1-Glycoproteins / Gene Deletion / Genome-Wide Association Study / DNA Copy Number Variations Type of study: Guideline / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Female / Humans / Pregnancy Language: En Journal: BMC Pregnancy Childbirth Journal subject: OBSTETRICIA Year: 2012 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pre-Eclampsia / Pregnancy-Specific beta 1-Glycoproteins / Gene Deletion / Genome-Wide Association Study / DNA Copy Number Variations Type of study: Guideline / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Female / Humans / Pregnancy Language: En Journal: BMC Pregnancy Childbirth Journal subject: OBSTETRICIA Year: 2012 Type: Article Affiliation country: United States