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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...
Autores principales: | Zhao, Linlu, Triche, Elizabeth W, Walsh, Kyle M, Bracken, Michael B, Saftlas, Audrey F, Hoh, Josephine, Dewan, Andrew T |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
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 |
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