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Human Genetics|March 1, 1990
Unusual X chromosome inactivation in a mentally retarded girl with an interstitial deletion Xq27: implications for the fragile X syndromeM Schmidt, A Certoma, D Du Sart, et al.The Journal of Clinical Investigation|January 1, 1990
Biochemical basis of prolidase deficiency. Polypeptide and RNA phenotypes and the relation to clinical phenotypesF Endo, A Tanoue, A Kitano, et al.The Journal of Pediatrics|October 1, 1977
Iminopeptiduria, skin ulcerations, and edema in a boy with prolidase deficiencyL J Sheffield, P Schlesinger, K Faull, et al.European Journal of Pediatrics|June 1, 1983
Heterogeneity of metatropic dysplasiaM Beck, M Roubicek, J G Rogers, et al.Journal of Inherited Metabolic Disease|January 1, 1990
Marfan syndrome: absence of type I or III collagen structural defects in 25 patientsV R Harley, D Chan, J G Rogers, et al.The Journal of Biological Chemistry|March 3, 1995
Type X collagen multimer assembly in vitro is prevented by a Gly618 to Val mutation in the alpha 1(X) NC1 domain resulting in Schmid metaphyseal chondrodysplasiaD Chan, W G Cole, J G Rogers, et al.Anaesthesia and Intensive Care|August 1, 1996
Anaesthesia for children with mucopolysaccharidosesC Moores, J G Rogers, I M McKenzie, et al.Annals of Neurology|March 1, 1996
Leigh syndrome: clinical features and biochemical and DNA abnormalitiesS Rahman, R B Blok, H H Dahl, et al.Molecular Genetics and Metabolism|November 14, 2000
Mutations in the 4-hydroxyphenylpyruvic acid dioxygenase gene are responsible for tyrosinemia type III and hawkinsinuriaK Tomoeda, H Awata, T Matsuura, et al.Teratology|February 1, 1986
Methacrylic acid as a teratogen in rat embryo cultureJ G Rogers, J C Greenaway, P E Mirkes, et al.Pageof 19