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C R Scott

Showing results (81-90 of 92) with videos related to

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The Journal of Clinical Investigation|December 1, 1985
An intragenic deletion of the factor IX gene in a family with hemophilia BS H Chen, S Yoshitake, P F Chance, et al.
American Journal of Epidemiology|March 1, 1995
Lactose and galactose intake and metabolism in relation to the risk of epithelial ovarian cancerL J Herrinton, N S Weiss, S A Beresford, et al.
American Journal of Medical Genetics|September 1, 1992
Hawkinsinuria in two familiesM Borden, J Holm, J Leslie, et al.
American Journal of Human Genetics|February 1, 1994
mtDNA and Y-chromosome polymorphisms in four Native American populations from southern MexicoA Torroni, Y S Chen, O Semino, et al.
The Journal of Pediatrics|February 1, 1974
Absence of erythrocyte adenosine deaminase associated with severe combined immunodeficiencyJ Yount, P Nichols, H D Ochs, et al.
Molecular Genetics and Metabolism|November 14, 2000
Mutations in the 4-hydroxyphenylpyruvic acid dioxygenase gene are responsible for tyrosinemia type III and hawkinsinuriaK Tomoeda, H Awata, T Matsuura, et al.
Fertility and Sterility|September 1, 1996
Lactose metabolism and time to pregnancyL J Herrinton, R N Lemaitre, S A Beresford, et al.
Journal of Acquired Immune Deficiency Syndromes|January 1, 1990
Adherence to Universal (barrier) Precautions during interventions on critically ill and injured emergency department patientsG D Kelen, T A DiGiovanna, D D Celentano, et al.
Journal of Inherited Metabolic Disease|March 10, 2007
Fabry disease: baseline medical characteristics of a cohort of 1765 males and females in the Fabry RegistryC M Eng, J Fletcher, W R Wilcox, et al.
Archives of Internal Medicine|September 17, 1998
Gaucher disease: recommendations on diagnosis, evaluation, and monitoringJ Charrow, J A Esplin, T J Gribble, et al.
Pageof 10

Showing results (81-90 of 92) with videos related to

Sort By:
Pageof 10
The Journal of Clinical Investigation|December 1, 1985
An intragenic deletion of the factor IX gene in a family with hemophilia BS H Chen, S Yoshitake, P F Chance, et al.
American Journal of Epidemiology|March 1, 1995
Lactose and galactose intake and metabolism in relation to the risk of epithelial ovarian cancerL J Herrinton, N S Weiss, S A Beresford, et al.
American Journal of Medical Genetics|September 1, 1992
Hawkinsinuria in two familiesM Borden, J Holm, J Leslie, et al.
American Journal of Human Genetics|February 1, 1994
mtDNA and Y-chromosome polymorphisms in four Native American populations from southern MexicoA Torroni, Y S Chen, O Semino, et al.
The Journal of Pediatrics|February 1, 1974
Absence of erythrocyte adenosine deaminase associated with severe combined immunodeficiencyJ Yount, P Nichols, H D Ochs, et al.
Molecular Genetics and Metabolism|November 14, 2000
Mutations in the 4-hydroxyphenylpyruvic acid dioxygenase gene are responsible for tyrosinemia type III and hawkinsinuriaK Tomoeda, H Awata, T Matsuura, et al.
Fertility and Sterility|September 1, 1996
Lactose metabolism and time to pregnancyL J Herrinton, R N Lemaitre, S A Beresford, et al.
Journal of Acquired Immune Deficiency Syndromes|January 1, 1990
Adherence to Universal (barrier) Precautions during interventions on critically ill and injured emergency department patientsG D Kelen, T A DiGiovanna, D D Celentano, et al.
Journal of Inherited Metabolic Disease|March 10, 2007
Fabry disease: baseline medical characteristics of a cohort of 1765 males and females in the Fabry RegistryC M Eng, J Fletcher, W R Wilcox, et al.
Archives of Internal Medicine|September 17, 1998
Gaucher disease: recommendations on diagnosis, evaluation, and monitoringJ Charrow, J A Esplin, T J Gribble, et al.
Pageof 10