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T M Cowan

Showing results (11-20 of 26) with videos related to

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Human Mutation|February 19, 2000
A missense mutation in the OCTN2 gene associated with residual carnitine transport activityY Wang, M A Kelly, T M Cowan, et al.
Maryland Medical Journal (Baltimore, Md. : 1985)|November 1, 1989
Recent advances in geneticsM G Blitzer, S Schwartz, T M Cowan, et al.
The Journal of Family Practice|August 3, 2000
The ultrasound-assisted physical examination in the periodic health evaluation of the elderlyT Siepel, D S Clifford, P A James, et al.
American Journal of Medical Genetics|November 15, 1993
Intrafamilial variability in Hurler syndrome and Sanfilippo syndrome type A: implications for evaluation of new therapiesG A McDowell, T M Cowan, M G Blitzer, et al.
The Journal of Family Practice|October 29, 1997
Family physicians' attitudes about and use of clinical practice guidelinesP A James, T M Cowan, R P Graham, et al.
Clinical Genetics|March 21, 2002
A PCR-based method for detecting known mutations in the human UDP galactose-4'-epimerase gene associated with epimerase-deficiency galactosemiaJ M Henderson, S M Huguenin, T M Cowan, et al.
Science (New York, N.Y.)|June 8, 1973
State-specific sciencesT M Cowan, C D Leake, A B Booth, et al.
The Journal of Rural Health : Official Journal of the American Rural Health Association and the National Rural Health Care Association|April 11, 2002
Readiness for Medicaid managed care reform initiatives: a profile of rural family physiciansP A James, T M Cowan, M K Bliss, et al.
Molecular Genetics and Metabolism|January 27, 2005
The urinary excretion of glutarylcarnitine is an informative tool in the biochemical diagnosis of glutaric acidemia type IS Tortorelli, S H Hahn, T M Cowan, et al.
American Journal of Human Genetics|October 27, 1997
Characterization of two mutations associated with epimerase-deficiency galactosemia, by use of a yeast expression system for human UDP-galactose-4-epimeraseB B Quimby, A Alano, S Almashanu, et al.
Pageof 3

Showing results (11-20 of 26) with videos related to

Sort By:
Pageof 3
Human Mutation|February 19, 2000
A missense mutation in the OCTN2 gene associated with residual carnitine transport activityY Wang, M A Kelly, T M Cowan, et al.
Maryland Medical Journal (Baltimore, Md. : 1985)|November 1, 1989
Recent advances in geneticsM G Blitzer, S Schwartz, T M Cowan, et al.
The Journal of Family Practice|August 3, 2000
The ultrasound-assisted physical examination in the periodic health evaluation of the elderlyT Siepel, D S Clifford, P A James, et al.
American Journal of Medical Genetics|November 15, 1993
Intrafamilial variability in Hurler syndrome and Sanfilippo syndrome type A: implications for evaluation of new therapiesG A McDowell, T M Cowan, M G Blitzer, et al.
The Journal of Family Practice|October 29, 1997
Family physicians' attitudes about and use of clinical practice guidelinesP A James, T M Cowan, R P Graham, et al.
Clinical Genetics|March 21, 2002
A PCR-based method for detecting known mutations in the human UDP galactose-4'-epimerase gene associated with epimerase-deficiency galactosemiaJ M Henderson, S M Huguenin, T M Cowan, et al.
Science (New York, N.Y.)|June 8, 1973
State-specific sciencesT M Cowan, C D Leake, A B Booth, et al.
The Journal of Rural Health : Official Journal of the American Rural Health Association and the National Rural Health Care Association|April 11, 2002
Readiness for Medicaid managed care reform initiatives: a profile of rural family physiciansP A James, T M Cowan, M K Bliss, et al.
Molecular Genetics and Metabolism|January 27, 2005
The urinary excretion of glutarylcarnitine is an informative tool in the biochemical diagnosis of glutaric acidemia type IS Tortorelli, S H Hahn, T M Cowan, et al.
American Journal of Human Genetics|October 27, 1997
Characterization of two mutations associated with epimerase-deficiency galactosemia, by use of a yeast expression system for human UDP-galactose-4-epimeraseB B Quimby, A Alano, S Almashanu, et al.
Pageof 3