High prevalence of three prothrombotic polymorphisms among Palestinians: factor V G1691A, factor II G20210A and methylenetetrahydrofolate reductase C677T
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cardiology and Cardiovascular Medicine,Hematology
Link
http://link.springer.com/content/pdf/10.1007/s11239-012-0731-9.pdf
Reference29 articles.
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4. Finan R, Tamim H, Ameen G et al (2002) Prevalence of factor VG1691A (factor V-leiden) and prothrombin gene mutations in a recurrent miscarriage population. Am J Hematol 71:300–305
5. Martinelli I, Taioli E, Cetin I, Marinoni A, Gerosa S, Villa MV, Bozzo M, Mannucci PM (2000) Mutations in coagulation factors in women with unexplained late fetal loss. N Engl J Med 343(14):1015–1018
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1. Association of inherited thrombophilia mutations and their combinations among palestinian women with unexplained recurrent miscarriage;Thrombosis Journal;2024-02-13
2. Association of Methylenetetrahydrofolate Reductase C677T and A1298C Gene Polymorphisms With Recurrent Pregnancy Loss in Syrian Women;Reproductive Sciences;2016-12-21
3. Global prevalence of prothrombin gene mutation G20210A and implications in women's health;Blood Coagulation & Fibrinolysis;2016-07
4. Frequency of three prothrombotic polymorphisms among Syrian population: factor V G1691A, prothrombin G20210A and methylenetetrahydrofolate reductase C677T;Annals of Human Biology;2015-12-10
5. Prothrombotic risk mutations and polymorphisms in patients with hemophilia A – a preliminary study / Polimorfismele și mutațiile cu risc protrombotic la pacienții cu hemofilie A - studiu preliminar;Romanian Review of Laboratory Medicine;2015-01-01
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