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Journal of Paediatrics and Child Health|February 1, 1990
Five cases demonstrating the distinctive behavioural features of chromosome deletion 17(p11.2 p11.2) (Smith-Magenis syndrome)A F Colley, M A Leversha, L E Voullaire, et al.Journal of Inherited Metabolic Disease|January 1, 1985
5,10-Methylenetetrahydrofolate reductase deficiency. Clinical and biochemical features of a further caseE A Haan, J G Rogers, G P Lewis, et al.Toxicology and Applied Pharmacology|February 1, 1984
Role of acrolein in cyclophosphamide teratogenicity in rat embryos in vitroP E Mirkes, J C Greenaway, J G Rogers, et al.Journal of Medical Genetics|September 1, 1990
The clinical features of osteogenesis imperfecta resulting from a non-functional carboxy terminal pro alpha 1(I) propeptide of type I procollagen and a severe deficiency of normal type I collagen in tissuesW G Cole, P E Campbell, J G Rogers, et al.Journal of Medical Genetics|April 1, 1990
The clinical features of three babies with osteogenesis imperfecta resulting from the substitution of glycine by arginine in the pro alpha 1(I) chain of type I procollagenW G Cole, C W Chow, J G Rogers, et al.The Journal of Pediatrics|February 1, 1977
A postaxial polydactyly-dental-vertebral syndromeJ G Rogers, L S Levin, J P Dorst, et al.The Journal of Pediatrics|June 1, 1987
Nonketotic hyperglycinemia: analyses of glycine cleavage system in typical and atypical casesK Hayasaka, K Tada, N Fueki, et al.The New England Journal of Medicine|February 26, 1976
Dihydrofolate reductase deficiency causing megaloblastic anemia in two familiesG P Tauro, D M Danks, P B Rowe, et al.Journal of Medical Genetics|September 11, 1998
Medical complications of achondroplasia: a multicentre patient reviewA G Hunter, A Bankier, J G Rogers, et al.Pageof 19