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Stephanie M Ware

Showing results (21-30 of 146) with videos related to

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Circulation. Cardiovascular Genetics|June 21, 2012
Modifying Mendel: approaches for identification of susceptibility alleles for human cardiovascular malformationsKim L McBride, Stephanie M Ware
Journal of Clinical & Experimental Cardiology|July 24, 2012
New Genetic Insights into Congenital Heart DiseaseStephanie M Ware, John Lynn Jefferies
Genes|April 27, 2024
Clinical Decision Analysis of Genetic Evaluation and Testing in 1013 Intensive Care Unit Infants with Congenital Heart Defects Supports Universal Genetic TestingBenjamin M Helm, Stephanie M Ware
Human Mutation|October 15, 2013
Genetic and functional analyses of ZIC3 variants in congenital heart diseaseJason Cowan, Muhammad Tariq, Stephanie M Ware
Pediatric Research|June 29, 2010
A mouse model of conduction system patterning abnormalities in heterotaxy syndromeRichard J Czosek, Allison Haaning, Stephanie M Ware
American Journal of Medical Genetics. Part A|April 9, 2009
High resolution SNP based microarray mapping of mosaic supernumerary marker chromosomes 13 and 17: delineating novel loci for apraxiaJillene M Kogan, Erin Miller, Stephanie M Ware
European Journal of Human Genetics : EJHG|October 28, 2005
Genetics of human heterotaxiasLirong Zhu, John W Belmont, Stephanie M Ware
Journal of Genetic Counseling|October 12, 2012
Uptake of cardiac screening and genetic testing among hypertrophic and dilated cardiomyopathy familiesErin M Miller, Yu Wang, Stephanie M Ware
Human Molecular Genetics|January 12, 2012
Preaxial polydactyly caused by Gli3 haploinsufficiency is rescued by Zic3 loss of function in miceMalgorzata E Quinn, Allison Haaning, Stephanie M Ware
Proceedings of the American Thoracic Society|September 20, 2011
Spectrum of clinical diseases caused by disorders of primary ciliaStephanie M Ware, Meral Gunay- Aygun, Friedhelm Hildebrandt
Pageof 15

Showing results (21-30 of 146) with videos related to

Sort By:
Pageof 15
Circulation. Cardiovascular Genetics|June 21, 2012
Modifying Mendel: approaches for identification of susceptibility alleles for human cardiovascular malformationsKim L McBride, Stephanie M Ware
Journal of Clinical & Experimental Cardiology|July 24, 2012
New Genetic Insights into Congenital Heart DiseaseStephanie M Ware, John Lynn Jefferies
Genes|April 27, 2024
Clinical Decision Analysis of Genetic Evaluation and Testing in 1013 Intensive Care Unit Infants with Congenital Heart Defects Supports Universal Genetic TestingBenjamin M Helm, Stephanie M Ware
Human Mutation|October 15, 2013
Genetic and functional analyses of ZIC3 variants in congenital heart diseaseJason Cowan, Muhammad Tariq, Stephanie M Ware
Pediatric Research|June 29, 2010
A mouse model of conduction system patterning abnormalities in heterotaxy syndromeRichard J Czosek, Allison Haaning, Stephanie M Ware
American Journal of Medical Genetics. Part A|April 9, 2009
High resolution SNP based microarray mapping of mosaic supernumerary marker chromosomes 13 and 17: delineating novel loci for apraxiaJillene M Kogan, Erin Miller, Stephanie M Ware
European Journal of Human Genetics : EJHG|October 28, 2005
Genetics of human heterotaxiasLirong Zhu, John W Belmont, Stephanie M Ware
Journal of Genetic Counseling|October 12, 2012
Uptake of cardiac screening and genetic testing among hypertrophic and dilated cardiomyopathy familiesErin M Miller, Yu Wang, Stephanie M Ware
Human Molecular Genetics|January 12, 2012
Preaxial polydactyly caused by Gli3 haploinsufficiency is rescued by Zic3 loss of function in miceMalgorzata E Quinn, Allison Haaning, Stephanie M Ware
Proceedings of the American Thoracic Society|September 20, 2011
Spectrum of clinical diseases caused by disorders of primary ciliaStephanie M Ware, Meral Gunay- Aygun, Friedhelm Hildebrandt
Pageof 15