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Journal of Inherited Metabolic Disease|January 1, 1987
Effect of the X-linked Hyp mutation on N-ethylmaleimide labelling of proteins in renal brush border membraneE J Vizel, H S Tenenhouse, C R Scriver
Human Genetics|January 1, 1984
Osteogenesis imperfecta: a heterogeneous morphologic phenotype in cultured dermal fibroblastsA P Boright, G A Lancaster, C R Scriver
Genetical Research|August 1, 1993
Parental origin of mutant allele does not explain absence of gene dose in X-linked Hyp miceZ Q Qiu, H S Tenenhouse, C R Scriver
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 Scriver
Clinical 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 Vizel
Biochimica Et Biophysica Acta|September 25, 1985
Transport competence of plasma membrane vesicles from cultured human fibroblastsJ A Buchanan, D S Rosenblatt, C R Scriver
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