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C R Scott

Showing results (51-60 of 92) with videos related to

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Journal of Cellular Physiology|July 1, 1977
Incorporation of purine nucleosides in cultured fibroblasts from a patient with purine nucleoside phosphorylase deficiency and associated T-cell immunodeficiencyW G Burke, S H Chen, C R Scott, et al.
American Journal of Human Genetics|November 1, 1977
Adenosine deaminase deficiency: another family with "silent" ADA allele and normal ADA activity in two heterozygotesS H Chen, C R Scott, E R Giblett, et al.
Journal of the American Veterinary Medical Association|December 29, 1999
Rabies in two privately owned domestic rabbitsB E Karp, N E Ball, C R Scott, et al.
The Journal of Pediatrics|January 1, 1971
Syndrome of accelerated skeletal maturation and relative failure to thrive: a newly recognized clinical growth disorderR E Marshall, C B Graham, C R Scott, et al.
Human Pathology|May 1, 1992
Gaucher's disease in the presence of normal glucocerebrosidase activityD E Schofield, C R Scott, J M Lage, et al.
Science (New York, N.Y.)|March 21, 1975
Absence of pyruvate decarboxylase activity in man: a cause of congenital lactic acidosisD F Farrell, A F Clark, C R Scott, et al.
The Journal of Pediatrics|November 1, 1970
Clinical and cellular studies of sarcosinemiaC R Scott, S H Clark, C C Teng, et al.
Human Molecular Genetics|May 1, 1993
Five novel factor IX mutations in unrelated hemophilia B familiesS H Chen, J M Schoof, C R Scott, et al.
The Journal of Pediatrics|July 1, 1996
Bone marrow transplantation in Hunter syndromeE J McKinnis, S Sulzbacher, J C Rutledge, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 17, 2006
The use of acarbose inhibition in the measurement of acid alpha-glucosidase activity in blood lymphocytes for the diagnosis of Pompe diseaseRhona M Jack, Cindy Gordon, C R Scott, et al.
Pageof 10

Showing results (51-60 of 92) with videos related to

Sort By:
Pageof 10
Journal of Cellular Physiology|July 1, 1977
Incorporation of purine nucleosides in cultured fibroblasts from a patient with purine nucleoside phosphorylase deficiency and associated T-cell immunodeficiencyW G Burke, S H Chen, C R Scott, et al.
American Journal of Human Genetics|November 1, 1977
Adenosine deaminase deficiency: another family with "silent" ADA allele and normal ADA activity in two heterozygotesS H Chen, C R Scott, E R Giblett, et al.
Journal of the American Veterinary Medical Association|December 29, 1999
Rabies in two privately owned domestic rabbitsB E Karp, N E Ball, C R Scott, et al.
The Journal of Pediatrics|January 1, 1971
Syndrome of accelerated skeletal maturation and relative failure to thrive: a newly recognized clinical growth disorderR E Marshall, C B Graham, C R Scott, et al.
Human Pathology|May 1, 1992
Gaucher's disease in the presence of normal glucocerebrosidase activityD E Schofield, C R Scott, J M Lage, et al.
Science (New York, N.Y.)|March 21, 1975
Absence of pyruvate decarboxylase activity in man: a cause of congenital lactic acidosisD F Farrell, A F Clark, C R Scott, et al.
The Journal of Pediatrics|November 1, 1970
Clinical and cellular studies of sarcosinemiaC R Scott, S H Clark, C C Teng, et al.
Human Molecular Genetics|May 1, 1993
Five novel factor IX mutations in unrelated hemophilia B familiesS H Chen, J M Schoof, C R Scott, et al.
The Journal of Pediatrics|July 1, 1996
Bone marrow transplantation in Hunter syndromeE J McKinnis, S Sulzbacher, J C Rutledge, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 17, 2006
The use of acarbose inhibition in the measurement of acid alpha-glucosidase activity in blood lymphocytes for the diagnosis of Pompe diseaseRhona M Jack, Cindy Gordon, C R Scott, et al.
Pageof 10