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Bailliere'S Clinical Haematology|September 1, 1995
Effects of folate deficiency on embryonic developmentB Christensen, D S RosenblattAmerican Journal of Human Genetics|December 1, 1996
Severe and mild mutations in cis for the methylenetetrahydrofolate reductase (MTHFR) gene, and description of five novel mutations in MTHFRP Goyette, B Christensen, D S Rosenblatt, et al.Pediatric Research|January 1, 1994
Effect of methionine and nitrous oxide on homocysteine export and remethylation in fibroblasts from cystathionine synthase-deficient, cb1G, and cb1E patientsB Christensen, D S Rosenblatt, R C Chu, et al.Human Mutation|February 19, 2000
Characterization of six novel mutations in the methylenetetrahydrofolate reductase (MTHFR) gene in patients with homocystinuriaS Sibani, B Christensen, E O'Ferrall, et al.Arteriosclerosis, Thrombosis, and Vascular Biology|March 1, 1997
Correlation of a common mutation in the methylenetetrahydrofolate reductase gene with plasma homocysteine in patients with premature coronary artery diseaseB Christensen, P Frosst, S Lussier-Cacan, et al.The Journal of Clinical Investigation|June 1, 1988
Genetic heterogeneity among patients with methylcobalamin deficiency. Definition of two complementation groups, cblE and cblGD Watkins, D S RosenblattAmerican Journal of Medical Genetics|November 1, 1989
Functional methionine synthase deficiency (cblE and cblG): clinical and biochemical heterogeneityD Watkins, D S RosenblattClinical and Investigative Medicine. Medecine Clinique Et Experimentale|April 1, 1991
Metabolic cooperation among cell lines from patients with inborn errors of vitamin B12 metabolism: differential response of cblC and cblDS Byck, D S RosenblattAmerican Journal of Human Genetics|September 1, 1986
Failure of lysosomal release of vitamin B12: a new complementation group causing methylmalonic aciduria (cblF)D Watkins, D S RosenblattBlood Reviews|September 1, 1987
Inherited disorders of vitamin B12 metabolismD S Rosenblatt, B A CooperPageof 140