Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

H A Taylor

Showing results (61-70 of 85) with videos related to

Pageof 9
Sort By:
American Journal of Medical Genetics|June 19, 1998
Constitutional del(19)(q12q13.1) in a three-year-old girl with severe phenotypic abnormalities affecting multiple organ systemsA S Kulharya, R C Michaelis, K S Norris, et al.
American Journal of Medical Genetics|July 1, 1983
Transport media for tissue specimens: a comparative studyW E Potts, R A Saul, S E Riley, et al.
Cytogenetics and Cell Genetics|January 1, 1991
Deletion mapping of plasminogen activator inhibitor, type I (PLANH1) and beta-glucuronidase (GUSB) in 7q21----q22C E Schwartz, P Stanislovitis, M C Phelan, et al.
The American Journal of Cardiology|November 17, 1998
Presenting characteristics, treatment patterns, and clinical outcomes of non-black minorities in the National Registry of Myocardial Infarction 2J G Canto, H A Taylor, W J Rogers, et al.
Journal of Child Neurology|June 1, 1997
beta-Galactosidase gene mutations in patients with slowly progressive GM1 gangliosidosisE M Kaye, C Shalish, J Livermore, et al.
Pediatrics|October 1, 1983
Sialic acid storage disease with sialuria: clinical and biochemical features in the severe infantile typeR E Stevenson, M Lubinsky, H A Taylor, et al.
Journal of the American College of Cardiology|February 1, 1997
Long-term survival of African Americans in the Coronary Artery Surgery Study (CASS)H A Taylor, M C Mickel, B R Chaitman, et al.
Circulation|June 1, 1989
Asymptomatic left main coronary artery disease in the Coronary Artery Surgery Study (CASS) registryH A Taylor, N J Deumite, B R Chaitman, et al.
Clinical Genetics|July 1, 1980
Duplication-deletion syndrome in a family with pericentric inversion of chromosome 6R J Schroer, D M Culp, R E Stevenson, et al.
Science (New York, N.Y.)|July 6, 1979
Comparison of calculated and measured ion densities on the dayside of venusA F Nagy, T E Cravens, R H Chen, et al.
Pageof 9

Showing results (61-70 of 85) with videos related to

Sort By:
Pageof 9
American Journal of Medical Genetics|June 19, 1998
Constitutional del(19)(q12q13.1) in a three-year-old girl with severe phenotypic abnormalities affecting multiple organ systemsA S Kulharya, R C Michaelis, K S Norris, et al.
American Journal of Medical Genetics|July 1, 1983
Transport media for tissue specimens: a comparative studyW E Potts, R A Saul, S E Riley, et al.
Cytogenetics and Cell Genetics|January 1, 1991
Deletion mapping of plasminogen activator inhibitor, type I (PLANH1) and beta-glucuronidase (GUSB) in 7q21----q22C E Schwartz, P Stanislovitis, M C Phelan, et al.
The American Journal of Cardiology|November 17, 1998
Presenting characteristics, treatment patterns, and clinical outcomes of non-black minorities in the National Registry of Myocardial Infarction 2J G Canto, H A Taylor, W J Rogers, et al.
Journal of Child Neurology|June 1, 1997
beta-Galactosidase gene mutations in patients with slowly progressive GM1 gangliosidosisE M Kaye, C Shalish, J Livermore, et al.
Pediatrics|October 1, 1983
Sialic acid storage disease with sialuria: clinical and biochemical features in the severe infantile typeR E Stevenson, M Lubinsky, H A Taylor, et al.
Journal of the American College of Cardiology|February 1, 1997
Long-term survival of African Americans in the Coronary Artery Surgery Study (CASS)H A Taylor, M C Mickel, B R Chaitman, et al.
Circulation|June 1, 1989
Asymptomatic left main coronary artery disease in the Coronary Artery Surgery Study (CASS) registryH A Taylor, N J Deumite, B R Chaitman, et al.
Clinical Genetics|July 1, 1980
Duplication-deletion syndrome in a family with pericentric inversion of chromosome 6R J Schroer, D M Culp, R E Stevenson, et al.
Science (New York, N.Y.)|July 6, 1979
Comparison of calculated and measured ion densities on the dayside of venusA F Nagy, T E Cravens, R H Chen, et al.
Pageof 9