A common mutation in the 5,10-methylenetetrahydrofolate reductase gene as a new risk factor for placental vasculopathy
- 1 May 2000
- journal article
- Published by Elsevier in American Journal of Obstetrics and Gynecology
- Vol. 182 (5) , 1258-1263
- https://doi.org/10.1067/mob.2000.105199
Abstract
No abstract availableKeywords
This publication has 18 references indexed in Scilit:
- Methylenetetrahydrofolate reductase polymorphism and pre-eclampsia.Journal of Medical Genetics, 1997
- Pracental abruption and its association with hypertension and prolonged rupture of membranes: A methodologic review and meta-analysisObstetrics & Gynecology, 1996
- Hyperhomocysteinemia as a Risk Factor for Deep-Vein ThrombosisNew England Journal of Medicine, 1996
- Underlying disorders associated with severe early-onset preeclampsiaAmerican Journal of Obstetrics and Gynecology, 1995
- A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductaseNature Genetics, 1995
- Placental Thrombi and Other Vascular LesionsPathology - Research and Practice, 1993
- Placental bed biopsies in placental abruptionBJOG: An International Journal of Obstetrics and Gynaecology, 1992
- Effects of sub-50 oral contraceptives on homocysteine metabolism: A preliminary studyContraception, 1992
- Multivitamin supplementation in oral contraceptive usersContraception, 1991
- Prevention of neural tube defects: Results of the Medical Research Council Vitamin StudyPublished by Elsevier ,1991