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C R Greenberg

Showing results (51-60 of 105) with videos related to

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Pediatrics|August 1, 1989
Newborn screening for galactosemia: a new method used in ManitobaC R Greenberg, L A Dilling, R Thompson, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|March 28, 2019
Hypophosphatasia: Canadian update on diagnosis and managementA A Khan, R Josse, P Kannu, et al.
The Journal of Biological Chemistry|June 15, 1988
Heterozygosity for a large deletion in the alpha 2(I) collagen gene has a dramatic effect on type I collagen secretion and produces perinatal lethal osteogenesis imperfectaM C Willing, D H Cohn, B Starman, et al.
American Journal of Medical Genetics|December 31, 1997
Low MSAFP levels and Williams syndromeB N Chodirker, C R Greenberg, N G Giddins, et al.
Anesthesiology|February 1, 1996
Comparison of the segregation of the RYR1 C1840T mutation with segregation of the caffeine/halothane contracture test results for malignant hyperthermia susceptibility in a large Manitoba Mennonite familyK D Serfas, D Bose, L Patel, et al.
Human Genetics|August 1, 1994
Linkage analysis of X-linked cleft palate and ankyloglossia in Manitoba Mennonite and British Columbia Native kindredsS M Gorski, K J Adams, P H Birch, et al.
Clinical Genetics|March 1, 1997
Two novel mutations in a Canadian family with aspartylglucosaminuria and early outcome post bone marrow transplantationA Laitinen, M Hietala, J C Haworth, et al.
Lancet (London, England)|August 20, 1988
Gene studies in newborn males with Duchenne muscular dystrophy detected by neonatal screeningC R Greenberg, M Rohringer, H K Jacobs, et al.
Journal of Inherited Metabolic Disease|October 27, 2004
Looking forward--an evidence-based approach to glutaryl-CoA dehydrogenase deficiencyS Kölker, P Burgard, J G Okun, et al.
Human Mutation|August 26, 1998
Glutaryl-CoA dehydrogenase mutations in glutaric acidemia (type I): review and report of thirty novel mutationsS I Goodman, D E Stein, S Schlesinger, et al.
Pageof 11

Showing results (51-60 of 105) with videos related to

Sort By:
Pageof 11
Pediatrics|August 1, 1989
Newborn screening for galactosemia: a new method used in ManitobaC R Greenberg, L A Dilling, R Thompson, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|March 28, 2019
Hypophosphatasia: Canadian update on diagnosis and managementA A Khan, R Josse, P Kannu, et al.
The Journal of Biological Chemistry|June 15, 1988
Heterozygosity for a large deletion in the alpha 2(I) collagen gene has a dramatic effect on type I collagen secretion and produces perinatal lethal osteogenesis imperfectaM C Willing, D H Cohn, B Starman, et al.
American Journal of Medical Genetics|December 31, 1997
Low MSAFP levels and Williams syndromeB N Chodirker, C R Greenberg, N G Giddins, et al.
Anesthesiology|February 1, 1996
Comparison of the segregation of the RYR1 C1840T mutation with segregation of the caffeine/halothane contracture test results for malignant hyperthermia susceptibility in a large Manitoba Mennonite familyK D Serfas, D Bose, L Patel, et al.
Human Genetics|August 1, 1994
Linkage analysis of X-linked cleft palate and ankyloglossia in Manitoba Mennonite and British Columbia Native kindredsS M Gorski, K J Adams, P H Birch, et al.
Clinical Genetics|March 1, 1997
Two novel mutations in a Canadian family with aspartylglucosaminuria and early outcome post bone marrow transplantationA Laitinen, M Hietala, J C Haworth, et al.
Lancet (London, England)|August 20, 1988
Gene studies in newborn males with Duchenne muscular dystrophy detected by neonatal screeningC R Greenberg, M Rohringer, H K Jacobs, et al.
Journal of Inherited Metabolic Disease|October 27, 2004
Looking forward--an evidence-based approach to glutaryl-CoA dehydrogenase deficiencyS Kölker, P Burgard, J G Okun, et al.
Human Mutation|August 26, 1998
Glutaryl-CoA dehydrogenase mutations in glutaric acidemia (type I): review and report of thirty novel mutationsS I Goodman, D E Stein, S Schlesinger, et al.
Pageof 11