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C R Greenberg

Showing results (41-50 of 105) with videos related to

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American Journal of Medical Genetics|April 1, 1992
New familial syndrome of unilateral upper eyelid coloboma, aberrant anterior hairline pattern, and anal anomalies in Manitoba IndiansS L Marles, C R Greenberg, T V Persaud, et al.
American Journal of Human Genetics|October 1, 1996
Limb-girdle muscular dystrophy and Miyoshi myopathy in an aboriginal Canadian kindred map to LGMD2B and segregate with the same haplotypeT Weiler, C R Greenberg, E Nylen, et al.
Human Genetics|October 1, 1993
Identification of an uncommon haptoglobin type using DNA and protein analysisS L Marles, P J McAlpine, T Zelinski, et al.
Clinical Biochemistry|August 17, 2010
LC-MS/MS progress in newborn screeningD C Lehotay, P Hall, J Lepage, et al.
Pediatric Radiology|January 1, 1991
Computer assisted analysis of hand radiographs in infantile hypophosphatasia carriersB N Chodirker, D Roy, C R Greenberg, et al.
Blood|June 15, 1990
Atypical presentation of Wiskott-Aldrich syndrome: diagnosis in two unrelated males based on studies of maternal T cell X chromosome inactivationJ M Puck, K A Siminovitch, M Poncz, et al.
The Journal of Pediatrics|March 10, 2001
Protein-sensitive and fasting hypoglycemia in children with the hyperinsulinism/hyperammonemia syndromeB Y Hsu, A Kelly, P S Thornton, 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|May 31, 2019
Correction to: Hypophosphatasia: Canadian update on diagnosis and managementA A Khan, R Josse, P Kannu, et al.
American Journal of Medical Genetics|June 1, 1992
Transmission of the fra(X) haplotype from three nonpenetrant brothers to their affected grandsonsA J Kirkilionis, A E Chudley, C R Greenberg, et al.
American Journal of Medical Genetics|March 1, 1988
A new autosomal recessive lethal chondrodystrophy with congenital hydropsC R Greenberg, D L Rimoin, H E Gruber, et al.
Pageof 11

Showing results (41-50 of 105) with videos related to

Sort By:
Pageof 11
American Journal of Medical Genetics|April 1, 1992
New familial syndrome of unilateral upper eyelid coloboma, aberrant anterior hairline pattern, and anal anomalies in Manitoba IndiansS L Marles, C R Greenberg, T V Persaud, et al.
American Journal of Human Genetics|October 1, 1996
Limb-girdle muscular dystrophy and Miyoshi myopathy in an aboriginal Canadian kindred map to LGMD2B and segregate with the same haplotypeT Weiler, C R Greenberg, E Nylen, et al.
Human Genetics|October 1, 1993
Identification of an uncommon haptoglobin type using DNA and protein analysisS L Marles, P J McAlpine, T Zelinski, et al.
Clinical Biochemistry|August 17, 2010
LC-MS/MS progress in newborn screeningD C Lehotay, P Hall, J Lepage, et al.
Pediatric Radiology|January 1, 1991
Computer assisted analysis of hand radiographs in infantile hypophosphatasia carriersB N Chodirker, D Roy, C R Greenberg, et al.
Blood|June 15, 1990
Atypical presentation of Wiskott-Aldrich syndrome: diagnosis in two unrelated males based on studies of maternal T cell X chromosome inactivationJ M Puck, K A Siminovitch, M Poncz, et al.
The Journal of Pediatrics|March 10, 2001
Protein-sensitive and fasting hypoglycemia in children with the hyperinsulinism/hyperammonemia syndromeB Y Hsu, A Kelly, P S Thornton, 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|May 31, 2019
Correction to: Hypophosphatasia: Canadian update on diagnosis and managementA A Khan, R Josse, P Kannu, et al.
American Journal of Medical Genetics|June 1, 1992
Transmission of the fra(X) haplotype from three nonpenetrant brothers to their affected grandsonsA J Kirkilionis, A E Chudley, C R Greenberg, et al.
American Journal of Medical Genetics|March 1, 1988
A new autosomal recessive lethal chondrodystrophy with congenital hydropsC R Greenberg, D L Rimoin, H E Gruber, et al.
Pageof 11