换一批Mutations in the gene for methylenetetrahydrofolate reductase, homocysteine levels, and vitamin status in women with a history of preeclampsia.
第一作者：
A M,Lachmeijer
第一单位：
Department of Clinical Genetics and Human Genetics, University Hospital Vrije Amsterdam, The Netherlands.
作者：
医学主题词
出生体重(Birth Weight);DNA(DNA);DNA引物(DNA Primers);脱氧核糖核酸酶类, 位点特异性Ⅱ型(Deoxyribonucleases, Type II Site-Specific);电泳, 聚丙烯酰氨凝胶(Electrophoresis, Polyacrylamide Gel);女(雌)性(Female);叶酸(Folic Acid);基因型(Genotype);孕龄(Gestational Age);HELLP综合征(HELLP Syndrome);高半胱氨酸(Homocysteine);人类(Humans);婴儿, 新生(Infant, Newborn);线性模型(Linear Models);甲硫氨酸(Methionine);亚甲基四氢叶酸还原酶(NADPH)(Methylenetetrahydrofolate Reductase (NADPH2));突变(Mutation);作用于CH-NH族供体的氧化还原酶类(Oxidoreductases Acting on CH-NH Group Donors);聚合酶链反应(Polymerase Chain Reaction);先兆子痫(Pre-Eclampsia);妊娠(Pregnancy);放射免疫测定(Radioimmunoassay);回归分析(Regression Analysis);维生素B12(Vitamin B 12)
DOI
10.1067/mob.2001.109393
PMID
11228493
发布时间
2019-06-16
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