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

BACKGROUND: 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 etiology of PE. METHODS: A genome-wide scan was performed...

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Detalles Bibliográficos
Autores principales: Zhao, Linlu, Triche, Elizabeth W, Walsh, Kyle M, Bracken, Michael B, Saftlas, Audrey F, Hoh, Josephine, Dewan, Andrew T
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3476390/
https://www.ncbi.nlm.nih.gov/pubmed/22748001
http://dx.doi.org/10.1186/1471-2393-12-61

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3476390/
https://www.ncbi.nlm.nih.gov/pubmed/22748001
http://dx.doi.org/10.1186/1471-2393-12-61

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