5,10-亚甲基四氢叶酸还原酶和胱硫醚β-合酶基因多态性作为阿尔及利亚塞蒂夫神经管缺陷的危险因素。关于Houcher等人的文章，《小儿神经外科学》2009年；45:472 - 477。 - Suppr

Polymorphisms of 5,10-Methylenetetrahydrofolate reductase and cystathionine beta-synthase genes as a risk factor for neural tube defects in Sétif, Algeria. Concerning the article by Houcher et al., Pediatr Neurosurg 2009;45:472-477.

George Timothy M

Dell Children's Medical Center, Austin, TX 78723, USA.

Pediatr Neurosurg. 2009;45(6):478. doi: 10.1159/000283087. Epub 2010 Feb 16.

Abstract

摘要

Pediatr Neurosurg. 2009;45(6):478. doi: 10.1159/000283087. Epub 2010 Feb 16.

Pediatr Neurosurg. 2009;45(6):472-7. doi: 10.1159/000283086. Epub 2010 Feb 16.

Birth Defects Res A Clin Mol Teratol. 2010 Aug;88(8):695-700. doi: 10.1002/bdra.20692.

J Hum Genet. 2001;46(3):105-9. doi: 10.1007/s100380170096.

Birth Defects Res A Clin Mol Teratol. 2008 Jul;82(7):540-2. doi: 10.1002/bdra.20454.

Mol Cell Probes. 2001 Apr;15(2):119-23. doi: 10.1006/mcpr.2001.0351.

Clin Appl Thromb Hemost. 2009 Oct;15(5):529-34. doi: 10.1177/1076029608319944. Epub 2008 Oct 7.

Zhonghua Fu Chan Ke Za Zhi. 2011 Apr;46(4):301-3.

Haematologica. 1999 Jun;84 Suppl EHA-4:53-6.

Zhonghua Liu Xing Bing Xue Za Zhi. 2006 Mar;27(3):260-3.

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