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Preeclampsia and cardiovascular disease share genetic risk factors on chromosome 2q22.

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第一作者: Mari,Løset
第一单位: Department of Cancer Research and Molecular Medicine, Norwegian University of Science and Technology (NTNU), N-7491 Trondheim, Norway. Electronic address: mari.loset@gmail.com.
作者单位: Department of Cancer Research and Molecular Medicine, Norwegian University of Science and Technology (NTNU), N-7491 Trondheim, Norway. Electronic address: mari.loset@gmail.com. [1] Department of Genetics, Texas Biomedical Research Institute, San Antonio, TX 78227, USA. [2] Centre for Genetic Origins of Health and Disease, The University of Western Australia, Perth, WA 6009, Australia. [3] School of Women's and Infants' Health, The University of Western Australia, Perth, WA 6009, Australia. [4] School of Medicine and Pharmacology, The University of Western Australia, Perth, WA 6000, Australia; Telethon Institute for Child Health Research, The University of Western Australia, Perth, WA 6008, Australia. [5] School of Medicine and Pharmacology, The University of Western Australia, Perth, WA 6000, Australia. [6] Department of Cancer Research and Molecular Medicine, Norwegian University of Science and Technology (NTNU), N-7491 Trondheim, Norway; Central Norway Regional Health Authority (RHA), N-7501 Stjørdal, Norway. [7] Department of Cancer Research and Molecular Medicine, Norwegian University of Science and Technology (NTNU), N-7491 Trondheim, Norway; Centre of Molecular Inflammation Research, Faculty of Medicine, Norwegian University of Science and Technology (NTNU), N-7491 Trondheim, Norway. [8] Department of Perinatal Medicine, Royal Women's Hospital, The University of Melbourne, Parkville, VIC 3052, Australia; Department of Obstetrics & Gynaecology, The University of Melbourne, Parkville, VIC 3052, Australia. [9]
DOI 10.1016/j.preghy.2014.03.005
PMID 26104425
发布时间 2015-06-24
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