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Birth Defects Original Article Series|June 1, 1971
The characterization of hereditary abnormalities of keratin: Clouston's ectodermal dysplasiaJ M Reynold, M B Gold, C R ScriverClinical and Investigative Medicine. Medecine Clinique Et Experimentale|August 1, 1991
Quantitation of beta-thalassemia genes in Quebec immigrants of Mediterranean, southeast Asian, and Asian Indian originsF Kaplan, G Kokotsis, A Capua, et al.American Journal of Medical Genetics|June 1, 1985
The effect of Mendelian disease on human health. II: Response to treatmentA Hayes, T Costa, C R Scriver, et al.The Biochemical Journal|August 15, 1980
Alkaline phosphatase activity does not mediate phosphate transport in the renal-cortical brush-border membraneH S Tenenhouse, C R Scriver, E J VizelBiochimica Et Biophysica Acta|September 25, 1985
Transport competence of plasma membrane vesicles from cultured human fibroblastsJ A Buchanan, D S Rosenblatt, C R ScriverPediatrics|December 1, 1981
Outcome of early and long-term management of classical maple syrup urine diseaseC L Clow, T M Reade, C R ScriverThe Biochemical Journal|August 15, 1983
Metabolism of ethylmalonate to mesaconate in the rat. Evidence for trans-dehydrogenation of methylsuccinateJ A Montgomery, O A Mamer, C R ScriverNucleic Acids Research|January 1, 1996
PAH Mutation Analysis Consortium Database: a database for disease-producing and other allelic variation at the human PAH locusL Hoang, S Byck, L Prevost, et al.Current Issues in Molecular Biology|August 8, 2001
Degradation of mutant proteins, underlying "loss of function" phenotypes, plays a major role in genetic diseaseP J WatersIn Vitro Cellular & Developmental Biology : Journal of the Tissue Culture Association|July 1, 1988
Initiation and characterization of primary mouse kidney epithelial culturesC L Bell, H S Tenenhouse, C R ScriverPageof 19