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C R Scott

Showing results (61-70 of 92) with videos related to

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American Journal of Human Genetics|April 1, 1989
Factor IXPortland: a nonsense mutation (CGA to TGA) resulting in hemophilia BS H Chen, C R Scott, J Schoof, et al.
Clinical Pediatrics|March 10, 1998
Non-insulin dependent diabetes mellitus in African-American youths of ArkansasC Pihoker, C R Scott, S Y Lensing, et al.
Human Genetics|June 1, 1991
CG dinucleotide transitions in the factor IX gene account for about half of the point mutations in hemophilia B patients: a Seattle seriesS H Chen, M Zhang, E W Lovrien, et al.
Journal of Comparative Pathology|January 26, 2013
Correlation of inflammation with adrenocortical atrophy in canine adrenalitisC B Frank, S Y Valentin, J C R Scott-Moncrieff, et al.
Lancet (London, England)|November 25, 1972
X-linked transmission of ornithine-transcarbamylase deficiencyC R Scott, C C Teng, S I Goodman, et al.
Gene Geography : a Computerized Bulletin on Human Gene Frequencies|April 1, 1997
Population genetics of the D4S139, D10S28, D17S74 and D17S79 VNTR loci among Asian, black, Caucasian, Hispanic and Native American populations from SeattleN Buroker, J Day, D Maclaren, et al.
American Journal of Human Genetics|November 1, 1978
Characterization of unusual hexosaminidase A (HEX A) deficient human mutantsJ S O'Brien, L Tennant, M L Veath, et al.
Nucleic Acids Research|March 11, 1991
Splice junction mutations in factor IX gene resulting in severe hemophilia BS H Chen, M Zhang, A R Thompson, et al.
Journal of Immunology (Baltimore, Md. : 1950)|June 1, 1979
Purine nucleoside phosphorylase deficiency: a molecular model for selective loss of T cell functionU H Ochs, S H Chen, H D Ochs, et al.
The Journal of Pediatrics|April 1, 1970
Cystathioninemia: a benign genetic conditionC R Scott, S W Dassell, S H Clark, et al.
Pageof 10

Showing results (61-70 of 92) with videos related to

Sort By:
Pageof 10
American Journal of Human Genetics|April 1, 1989
Factor IXPortland: a nonsense mutation (CGA to TGA) resulting in hemophilia BS H Chen, C R Scott, J Schoof, et al.
Clinical Pediatrics|March 10, 1998
Non-insulin dependent diabetes mellitus in African-American youths of ArkansasC Pihoker, C R Scott, S Y Lensing, et al.
Human Genetics|June 1, 1991
CG dinucleotide transitions in the factor IX gene account for about half of the point mutations in hemophilia B patients: a Seattle seriesS H Chen, M Zhang, E W Lovrien, et al.
Journal of Comparative Pathology|January 26, 2013
Correlation of inflammation with adrenocortical atrophy in canine adrenalitisC B Frank, S Y Valentin, J C R Scott-Moncrieff, et al.
Lancet (London, England)|November 25, 1972
X-linked transmission of ornithine-transcarbamylase deficiencyC R Scott, C C Teng, S I Goodman, et al.
Gene Geography : a Computerized Bulletin on Human Gene Frequencies|April 1, 1997
Population genetics of the D4S139, D10S28, D17S74 and D17S79 VNTR loci among Asian, black, Caucasian, Hispanic and Native American populations from SeattleN Buroker, J Day, D Maclaren, et al.
American Journal of Human Genetics|November 1, 1978
Characterization of unusual hexosaminidase A (HEX A) deficient human mutantsJ S O'Brien, L Tennant, M L Veath, et al.
Nucleic Acids Research|March 11, 1991
Splice junction mutations in factor IX gene resulting in severe hemophilia BS H Chen, M Zhang, A R Thompson, et al.
Journal of Immunology (Baltimore, Md. : 1950)|June 1, 1979
Purine nucleoside phosphorylase deficiency: a molecular model for selective loss of T cell functionU H Ochs, S H Chen, H D Ochs, et al.
The Journal of Pediatrics|April 1, 1970
Cystathioninemia: a benign genetic conditionC R Scott, S W Dassell, S H Clark, et al.
Pageof 10