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Circulation. Cardiovascular Genetics
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June 21, 2012
Modifying Mendel: approaches for identification of susceptibility alleles for human cardiovascular malformations
Kim L McBride, Stephanie M Ware
Journal of Clinical & Experimental Cardiology
|
July 24, 2012
New Genetic Insights into Congenital Heart Disease
Stephanie 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 Testing
Benjamin M Helm, Stephanie M Ware
Human Mutation
|
October 15, 2013
Genetic and functional analyses of ZIC3 variants in congenital heart disease
Jason Cowan, Muhammad Tariq, Stephanie M Ware
Pediatric Research
|
June 29, 2010
A mouse model of conduction system patterning abnormalities in heterotaxy syndrome
Richard 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 apraxia
Jillene M Kogan, Erin Miller, Stephanie M Ware
European Journal of Human Genetics : EJHG
|
October 28, 2005
Genetics of human heterotaxias
Lirong 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 families
Erin 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 mice
Malgorzata 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 cilia
Stephanie M Ware, Meral Gunay- Aygun, Friedhelm Hildebrandt
Page
of 15
Search research articles
Search
Showing results (21-30 of 146) with videos related to
Sort By:
Page
of 15
Circulation. Cardiovascular Genetics
|
June 21, 2012
Modifying Mendel: approaches for identification of susceptibility alleles for human cardiovascular malformations
Kim L McBride, Stephanie M Ware
Journal of Clinical & Experimental Cardiology
|
July 24, 2012
New Genetic Insights into Congenital Heart Disease
Stephanie 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 Testing
Benjamin M Helm, Stephanie M Ware
Human Mutation
|
October 15, 2013
Genetic and functional analyses of ZIC3 variants in congenital heart disease
Jason Cowan, Muhammad Tariq, Stephanie M Ware
Pediatric Research
|
June 29, 2010
A mouse model of conduction system patterning abnormalities in heterotaxy syndrome
Richard 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 apraxia
Jillene M Kogan, Erin Miller, Stephanie M Ware
European Journal of Human Genetics : EJHG
|
October 28, 2005
Genetics of human heterotaxias
Lirong 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 families
Erin 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 mice
Malgorzata 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 cilia
Stephanie M Ware, Meral Gunay- Aygun, Friedhelm Hildebrandt
Page
of 15