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Stephanie M Ware

Showing results (41-50 of 146) with videos related to

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Genes|August 27, 2021
Genetic Evaluation of Inpatient Neonatal and Infantile Congenital Heart Defects: New Findings and Review of the LiteratureBenjamin M Helm, Benjamin J Landis, Stephanie M Ware
Neural Development|August 18, 2017
Septal contributions to olfactory bulb interneuron diversity in the embryonic mouse telencephalon: role of the homeobox gene Gsx2Shenyue Qin, Stephanie M Ware, Ronald R Waclaw, et al.
Human Molecular Genetics|December 23, 2006
Nuclear import and export signals are essential for proper cellular trafficking and function of ZIC3James E J Bedard, Jennifer D Purnell, Stephanie M Ware
American Journal of Medical Genetics. Part A|February 7, 2012
Implications for genotype-phenotype predictions in Townes-Brocks syndrome: case report of a novel SALL1 deletion and review of the literatureErin M Miller, Robert Hopkin, Liming Bao, et al.
Plos One|August 23, 2011
Identification of a novel ZIC3 isoform and mutation screening in patients with heterotaxy and congenital heart diseaseJames E J Bedard, Allison M Haaning, Stephanie M Ware
Molecular Genetics and Metabolism|May 25, 2012
Recessive deoxyguanosine kinase deficiency causes juvenile onset mitochondrial myopathyAdam H Buchaklian, Daniel Helbling, Stephanie M Ware, et al.
Current Opinion in Cardiology|April 21, 2004
Molecular genetics of heterotaxy syndromesJohn W Belmont, Bhagyalaxmi Mohapatra, Jeffrey A Towbin, et al.
World Journal for Pediatric & Congenital Heart Surgery|June 9, 2025
Report of Facing Heterotaxy Together 2024: A Virtual, Multidisciplinary Scientific ConferenceThomas G Saba, David N Schidlow, Necia Sabin, et al.
Circulation. Genomic and Precision Medicine|March 28, 2025
Dysmorphology-Based Prediction Model for Genetic Disorders in Infants With Congenital Heart DiseaseBenjamin M Helm, Leah Wetherill, Benjamin J Landis, et al.
Scientific Reports|January 19, 2017
Molecular Characterization of Pediatric Restrictive Cardiomyopathy from Integrative GenomicsTara N Rindler, Robert B Hinton, Nathan Salomonis, et al.
Pageof 15

Showing results (41-50 of 146) with videos related to

Sort By:
Pageof 15
Genes|August 27, 2021
Genetic Evaluation of Inpatient Neonatal and Infantile Congenital Heart Defects: New Findings and Review of the LiteratureBenjamin M Helm, Benjamin J Landis, Stephanie M Ware
Neural Development|August 18, 2017
Septal contributions to olfactory bulb interneuron diversity in the embryonic mouse telencephalon: role of the homeobox gene Gsx2Shenyue Qin, Stephanie M Ware, Ronald R Waclaw, et al.
Human Molecular Genetics|December 23, 2006
Nuclear import and export signals are essential for proper cellular trafficking and function of ZIC3James E J Bedard, Jennifer D Purnell, Stephanie M Ware
American Journal of Medical Genetics. Part A|February 7, 2012
Implications for genotype-phenotype predictions in Townes-Brocks syndrome: case report of a novel SALL1 deletion and review of the literatureErin M Miller, Robert Hopkin, Liming Bao, et al.
Plos One|August 23, 2011
Identification of a novel ZIC3 isoform and mutation screening in patients with heterotaxy and congenital heart diseaseJames E J Bedard, Allison M Haaning, Stephanie M Ware
Molecular Genetics and Metabolism|May 25, 2012
Recessive deoxyguanosine kinase deficiency causes juvenile onset mitochondrial myopathyAdam H Buchaklian, Daniel Helbling, Stephanie M Ware, et al.
Current Opinion in Cardiology|April 21, 2004
Molecular genetics of heterotaxy syndromesJohn W Belmont, Bhagyalaxmi Mohapatra, Jeffrey A Towbin, et al.
World Journal for Pediatric & Congenital Heart Surgery|June 9, 2025
Report of Facing Heterotaxy Together 2024: A Virtual, Multidisciplinary Scientific ConferenceThomas G Saba, David N Schidlow, Necia Sabin, et al.
Circulation. Genomic and Precision Medicine|March 28, 2025
Dysmorphology-Based Prediction Model for Genetic Disorders in Infants With Congenital Heart DiseaseBenjamin M Helm, Leah Wetherill, Benjamin J Landis, et al.
Scientific Reports|January 19, 2017
Molecular Characterization of Pediatric Restrictive Cardiomyopathy from Integrative GenomicsTara N Rindler, Robert B Hinton, Nathan Salomonis, et al.
Pageof 15