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Bruce D Gelb

Showing results (11-20 of 284) with videos related to

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European Journal of Medical Genetics|August 2, 2005
Germ-line and somatic PTPN11 mutations in human diseaseMarco Tartaglia, Bruce D Gelb
The Journal of Clinical Investigation|February 23, 2011
RAS signaling pathway mutations and hypertrophic cardiomyopathy: getting into and out of the thick of itBruce D Gelb, Marco Tartaglia
American Journal of Medical Genetics. Part A|November 28, 2020
A de novo pathogenic BMP2 variant-related phenotype with the novel finding of bicuspid aortic valveNeha Ahluwalia, Bruce D Gelb
Annals of the New York Academy of Sciences|October 21, 2010
Disorders of dysregulated signal traffic through the RAS-MAPK pathway: phenotypic spectrum and molecular mechanismsMarco Tartaglia, Bruce D Gelb
Human Molecular Genetics|September 22, 2006
Noonan syndrome and related disorders: dysregulated RAS-mitogen activated protein kinase signal transductionBruce D Gelb, Marco Tartaglia
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|February 6, 2020
Congenital heart defects in Noonan syndrome: Diagnosis, management, and treatmentLéa Linglart, Bruce D Gelb
Circulation. Cardiovascular Genetics|June 21, 2012
The Good SHP2 Association: a porthole into the genetics of congenital heart diseaseBruce D Gelb, Christine E Seidman
Current Opinion in Cardiology|April 7, 2007
The genetics of congenital heart disease: a review of recent developmentsConstance G Weismann, Bruce D Gelb
Current Opinion in Cardiology|February 13, 2016
Genetics of congenital heart diseaseJonathan J Edwards, Bruce D Gelb
Cold Spring Harbor Perspectives in Medicine|July 3, 2014
Complex genetics and the etiology of human congenital heart diseaseBruce D Gelb, Wendy K Chung
Pageof 29

Showing results (11-20 of 284) with videos related to

Sort By:
Pageof 29
European Journal of Medical Genetics|August 2, 2005
Germ-line and somatic PTPN11 mutations in human diseaseMarco Tartaglia, Bruce D Gelb
The Journal of Clinical Investigation|February 23, 2011
RAS signaling pathway mutations and hypertrophic cardiomyopathy: getting into and out of the thick of itBruce D Gelb, Marco Tartaglia
American Journal of Medical Genetics. Part A|November 28, 2020
A de novo pathogenic BMP2 variant-related phenotype with the novel finding of bicuspid aortic valveNeha Ahluwalia, Bruce D Gelb
Annals of the New York Academy of Sciences|October 21, 2010
Disorders of dysregulated signal traffic through the RAS-MAPK pathway: phenotypic spectrum and molecular mechanismsMarco Tartaglia, Bruce D Gelb
Human Molecular Genetics|September 22, 2006
Noonan syndrome and related disorders: dysregulated RAS-mitogen activated protein kinase signal transductionBruce D Gelb, Marco Tartaglia
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|February 6, 2020
Congenital heart defects in Noonan syndrome: Diagnosis, management, and treatmentLéa Linglart, Bruce D Gelb
Circulation. Cardiovascular Genetics|June 21, 2012
The Good SHP2 Association: a porthole into the genetics of congenital heart diseaseBruce D Gelb, Christine E Seidman
Current Opinion in Cardiology|April 7, 2007
The genetics of congenital heart disease: a review of recent developmentsConstance G Weismann, Bruce D Gelb
Current Opinion in Cardiology|February 13, 2016
Genetics of congenital heart diseaseJonathan J Edwards, Bruce D Gelb
Cold Spring Harbor Perspectives in Medicine|July 3, 2014
Complex genetics and the etiology of human congenital heart diseaseBruce D Gelb, Wendy K Chung
Pageof 29