期刊文献+

MTHFR基因型多态性与反复自然流产相关性的研究

原文传递
导出
摘要 目的研究N5,N10-亚甲基四氢叶酸还原酶(5,10-methylenetetrahydro-folate reductase,MTHFR)基因位点C677T的多态性与反复自然流产(recurrent spontaneous abortion,RSA)发生的关系。方法采用聚合酶链反应-限制性片段长度多态(PCR-RFLP)技术检测134例RSA患者和126例正常妇女MTHFR基因C677T位点的分布和频率。结果①RSA组T/T型出现频率高于对照组,C/C型以及C/T+T/T型频率两组没有显著差异。②RSA组的T等位基因频率高于对照组。结论 MTHFR基因位点T/T型突变是RSA的危险因素。
出处 《中国优生与遗传杂志》 2012年第12期38-39,共2页 Chinese Journal of Birth Health & Heredity
  • 相关文献

参考文献8

  • 1Regan L, Rai R. Epidemiology and the medical causes of miscarriage [ J]. Baillieres Best Pract Res Clin Obstet Gynaecol,2000,14:839 - 854. 被引量:1
  • 2Rey E, Kahn SR, David M, et al. Theombophilic disorders and fetal loss. A meta -analysis[ J]. Lancetr,2003 ,361:901 -908. 被引量:1
  • 3Lipoprotein (a) and other prothrombotic risk factor in Causasian women with unexplained recurrent miscarriage. Results of a muhicen- tre case - control study [ J ]. Thromb Haemost, 2005,93 ( 5 ) : 867 - 871. 被引量:1
  • 4Gueant JL, Candito M, Andres E, Van OE, et al. Familial pernicious anaemia with hyperhomocysteinaemia in recurrent early pregnancy loss [ J]. Thromb Haemost ,2004,92 ( 5 ) : 1147 - 9. 被引量:1
  • 5Fodinger M, Hor WH, Sunder - Plassmann G. Molecular biology of 5, 10 - methylenetetnahydrofolate reductase [ J ]. Nephrol, 2000,13 ( 1 ) : 20 -33. 被引量:1
  • 6Candito M, Magnaldo S, Bayle J, et al. Clinical B12 deficiency in one case of recurrentspontaneous pregnancy loss [ J ]. Clin Chem Lab Med ,2003,41 (8) : 1026 - 1027. 被引量:1
  • 7Isotalo PA, Wells GA, Donnelly JG. Neonatal and fetal methylenetet- rahydrofolate reductase genetic polyorphisms: an examination of C667T and A1298C mutations[J]. Am J Hum Gnete,2000,67(4) : 986 - 990. 被引量:1
  • 8Van der Molen EF,Arends GE,Nelen WL,et al. A common mutation in the 5,10 -methylenetetrahydrofolate reductase gene as a new risk Factor for placental vasculopathy [ J ]. Am J Obstet Gyneco1,2000,182 (5) : 1258 - 1263. 被引量:1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部