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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Dec 10, 2024. (Total: 234259Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Abruptio Placentae and MTHFR[original query]
Combined heterozygosity for methylenetetrahydrofolate reductase (MTHFR) mutations C677T and A1298C is associated with abruptio placentae but not with intrauterine growth restriction.
European journal of obstetrics, gynecology, and reproductive biology 2001 Aug 97 (2): 174-7.
Gebhardt GS, Scholtz CL, Hillermann R, Odendaal HJ
MTHFD1 R653Q polymorphism is a maternal genetic risk factor for severe abruptio placentae.
American journal of medical genetics. Part A 2005 Feb 132A (4): 365-8.
Parle-McDermott Anne, Mills James L, Kirke Peadar N, Cox Christopher, Signore Caroline C, Kirke Sandra, Molloy Anne M, O'Leary Valerie B, Pangilinan Faith J, O'Herlihy Colm, Brody Lawrence C, Scott John
The effect of hereditary thrombophilia on recurrent pregnancy loss: a retrospective cohort study.
BMC pregnancy and childbirth 2024 11 24 (1): 719.
Hasan Berkan Sayal, Mehmet Sinan Beks
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