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B J Clark

Showing results (181-190 of 188) with videos related to

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Nature Medicine|November 1, 1995
A pilot study of ex vivo gene therapy for homozygous familial hypercholesterolaemiaM Grossman, D J Rader, D W Muller, et al.
Pediatrics|May 11, 1997
Detection of a 22q11.2 deletion in cardiac patients suggests a risk for velopharyngeal incompetenceD M McDonald-McGinn, D A Driscoll, B S Emanuel, et al.
Molecular and Cellular Endocrinology|May 30, 2001
Elements involved in the regulation of the StAR geneD M Stocco, B J Clark, A J Reinhart, et al.
American Journal of Human Genetics|September 29, 2000
Chromosomal duplication involving the forkhead transcription factor gene FOXC1 causes iris hypoplasia and glaucomaO J Lehmann, N D Ebenezer, T Jordan, et al.
Journal of the American College of Cardiology|August 26, 1998
Frequency of 22q11 deletions in patients with conotruncal defectsE Goldmuntz, B J Clark, L E Mitchell, et al.
American Journal of Medical Genetics|July 16, 1999
Cognitive and behavior profile of preschool children with chromosome 22q11.2 deletionM Gerdes, C Solot, P P Wang, et al.
American Heart Journal|October 2, 2001
Design and baseline characteristics for the ACE Inhibitor After Anthracycline (AAA) study of cardiac dysfunction in long-term pediatric cancer survivorsJ H Silber, A Cnaan, B J Clark, et al.
Genetic Testing|January 1, 1997
The 22q11.2 deletion: screening, diagnostic workup, and outcome of results; report on 181 patientsD M McDonald-McGinn, D LaRossa, E Goldmuntz, et al.
Pageof 19

Showing results (181-190 of 188) with videos related to

Sort By:
Pageof 19
You have reached the last page of results.This site can display upto 188 results.
Nature Medicine|November 1, 1995
A pilot study of ex vivo gene therapy for homozygous familial hypercholesterolaemiaM Grossman, D J Rader, D W Muller, et al.
Pediatrics|May 11, 1997
Detection of a 22q11.2 deletion in cardiac patients suggests a risk for velopharyngeal incompetenceD M McDonald-McGinn, D A Driscoll, B S Emanuel, et al.
Molecular and Cellular Endocrinology|May 30, 2001
Elements involved in the regulation of the StAR geneD M Stocco, B J Clark, A J Reinhart, et al.
American Journal of Human Genetics|September 29, 2000
Chromosomal duplication involving the forkhead transcription factor gene FOXC1 causes iris hypoplasia and glaucomaO J Lehmann, N D Ebenezer, T Jordan, et al.
Journal of the American College of Cardiology|August 26, 1998
Frequency of 22q11 deletions in patients with conotruncal defectsE Goldmuntz, B J Clark, L E Mitchell, et al.
American Journal of Medical Genetics|July 16, 1999
Cognitive and behavior profile of preschool children with chromosome 22q11.2 deletionM Gerdes, C Solot, P P Wang, et al.
American Heart Journal|October 2, 2001
Design and baseline characteristics for the ACE Inhibitor After Anthracycline (AAA) study of cardiac dysfunction in long-term pediatric cancer survivorsJ H Silber, A Cnaan, B J Clark, et al.
Genetic Testing|January 1, 1997
The 22q11.2 deletion: screening, diagnostic workup, and outcome of results; report on 181 patientsD M McDonald-McGinn, D LaRossa, E Goldmuntz, et al.
Pageof 19