المؤلفون: Afman LA; University Medical Center Nijmegen, Department of Pediatrics, Laboratory of Pediatrics and Neurology, P.O. Box 9101, 6500 HB Nijmegen, The Netherlands., Lievers KJ, van der Put NM, Trijbels FJ, Blom HJ

المصدر: European journal of human genetics : EJHG [Eur J Hum Genet] 2002 Jul; Vol. 10 (7), pp. 433-8.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 9302235 Publication Model: Print Cited Medium: Print ISSN: 1018-4813 (Print) Linking ISSN: 10184813 NLM ISO Abbreviation: Eur J Hum Genet Subsets: MEDLINE

مواضيع طبية MeSH: Polymorphism, Single Nucleotide*, Neural Tube Defects/*genetics , Transcobalamins/*genetics , Transcobalamins/*metabolism, Adult ; Amino Acid Substitution ; Female ; Gene Frequency ; Humans ; Netherlands ; Odds Ratio ; Sequence Analysis, DNA ; Vitamin B 12/metabolism ; White People