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F R Goodman

Showing results (41-50 of 52) with videos related to

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Pharmacology|January 1, 1988
Effects of two nonsulfhydryl angiotensin-converting enzyme inhibitors, CGS 14831 and CGS 16617, on myocardial damage and left-ventricular hypertrophy following coronary artery occlusion in the ratE F Smith, J W Egan, F R Goodman, et al.
The Journal of Pharmacology and Experimental Therapeutics|September 1, 1987
Pharmacological characterization of CGS 15943A: a novel nonxanthine adenosine antagonistG Ghai, J E Francis, M Williams, et al.
Nature Genetics|May 20, 1998
Mutation and deletion of the pseudoautosomal gene SHOX cause Leri-Weill dyschondrosteosisD J Shears, H J Vassal, F R Goodman, et al.
European Journal of Human Genetics : EJHG|August 22, 2000
Physical map of a 1.5 mb region on 12p11.2 harbouring a synpolydactyly associated chromosomal breakpointP Debeer, E F Schoenmakers, R Thoelen, et al.
Journal of Medical Genetics|May 23, 2001
A novel acropectoral syndrome maps to chromosome 7q36M Dundar, T M Gordon, I Ozyazgan, et al.
European Journal of Pediatrics|December 14, 1999
Sacral dysgenesis associated with terminal deletion of chromosome 7q: a report of two familiesJ Wang, L Spitz, R Hayward, et al.
American Journal of Medical Genetics|April 6, 1999
Acromelic frontonasal dysostosisS F Slaney, F R Goodman, B L Eilers-Walsman, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 8, 1997
Synpolydactyly phenotypes correlate with size of expansions in HOXD13 polyalanine tractF R Goodman, S Mundlos, Y Muragaki, et al.
American Journal of Human Genetics|June 7, 2000
Novel HOXA13 mutations and the phenotypic spectrum of hand-foot-genital syndromeF R Goodman, C Bacchelli, A F Brady, et al.
Nature Genetics|September 1, 1997
Mutations in CDMP1 cause autosomal dominant brachydactyly type CA Polinkovsky, N H Robin, J T Thomas, et al.
Pageof 6

Showing results (41-50 of 52) with videos related to

Sort By:
Pageof 6
Pharmacology|January 1, 1988
Effects of two nonsulfhydryl angiotensin-converting enzyme inhibitors, CGS 14831 and CGS 16617, on myocardial damage and left-ventricular hypertrophy following coronary artery occlusion in the ratE F Smith, J W Egan, F R Goodman, et al.
The Journal of Pharmacology and Experimental Therapeutics|September 1, 1987
Pharmacological characterization of CGS 15943A: a novel nonxanthine adenosine antagonistG Ghai, J E Francis, M Williams, et al.
Nature Genetics|May 20, 1998
Mutation and deletion of the pseudoautosomal gene SHOX cause Leri-Weill dyschondrosteosisD J Shears, H J Vassal, F R Goodman, et al.
European Journal of Human Genetics : EJHG|August 22, 2000
Physical map of a 1.5 mb region on 12p11.2 harbouring a synpolydactyly associated chromosomal breakpointP Debeer, E F Schoenmakers, R Thoelen, et al.
Journal of Medical Genetics|May 23, 2001
A novel acropectoral syndrome maps to chromosome 7q36M Dundar, T M Gordon, I Ozyazgan, et al.
European Journal of Pediatrics|December 14, 1999
Sacral dysgenesis associated with terminal deletion of chromosome 7q: a report of two familiesJ Wang, L Spitz, R Hayward, et al.
American Journal of Medical Genetics|April 6, 1999
Acromelic frontonasal dysostosisS F Slaney, F R Goodman, B L Eilers-Walsman, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 8, 1997
Synpolydactyly phenotypes correlate with size of expansions in HOXD13 polyalanine tractF R Goodman, S Mundlos, Y Muragaki, et al.
American Journal of Human Genetics|June 7, 2000
Novel HOXA13 mutations and the phenotypic spectrum of hand-foot-genital syndromeF R Goodman, C Bacchelli, A F Brady, et al.
Nature Genetics|September 1, 1997
Mutations in CDMP1 cause autosomal dominant brachydactyly type CA Polinkovsky, N H Robin, J T Thomas, et al.
Pageof 6