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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Dec 10, 2023. (Total: 223917Documents)
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Records 1 - 4 (of 4 Records)

Query Trace: Pregnancy Complications and F5[original query]
Polymorphisms of thrombophilic and vasoactive genes and severe preeclampsia: a pilot study.
Journal of the Society for Gynecologic Investigation 2004 May 11 (4): 227-31.
Tempfer Clemens B, Jirecek Stefan, Riener Eva-Katrin, Zeisler Harald, Denschlag Dominik, Hefler Lukas, Husslein Peter
The association of inherited thrombophilia and intrauterine fetal death: a case-control study.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2011 Dec 22 (8): 8.
Helgadottir LB, Skjeldestad FE, Jacobsen AF, Sandset PM, Jacobsen EM
Detection of human genome mutations associated with pregnancy complications using 3-D microarray based on macroporous polymer monoliths.
Talanta 2016 Jan 147 537-46.
Glotov A S, Sinitsyna E S, Danilova M M, Vashukova E S, Walter J G, Stahl F, Baranov V S, Vlakh E G, Tennikova T
Genetic markers for inherited thrombophilia related pregnancy loss and implantation failure in Indian population - implications for diagnosis and clinical management.
The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians 2022 2 35 (25): 9406-9414.
Udumudi Anuradha, Lava Chait
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