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Gregory Costain

Showing results (41-50 of 144) with videos related to

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European Journal of Human Genetics : EJHG|September 6, 2022
Developmental implications of genetic testing for physical indicationsDanielle A Baribeau, Ny Hoang, Thanuja Selvanayagam, et al.
Seizure|October 5, 2023
Drug-resistant focal epilepsy in a girl with SETD5-related intellectual disabilityRanjith Kumar Manokaran, Ayako Ochi, Elizabeth Kerr, et al.
European Journal of Human Genetics : EJHG|November 27, 2023
Estimating the proportion of nonsense variants undergoing the newly described phenomenon of manufactured splice rescueBushra Haque, David Cheerie, Saba Birkadze, et al.
International Journal of Cardiology|December 15, 2015
Genome-wide rare copy number variations contribute to genetic risk for transposition of the great arteriesGregory Costain, Anath C Lionel, Lucas Ogura, et al.
Schizophrenia Bulletin|December 14, 2012
Evaluating genetic counseling for individuals with schizophrenia in the molecular ageGregory Costain, Mary Jane Esplen, Brenda Toner, et al.
Molecular Genetics and Metabolism Reports|November 22, 2017
Enzyme replacement therapy in perinatal hypophosphatasia: Case report of a negative outcome and lessons for clinical practiceGregory Costain, Aideen M Moore, Lauren Munroe, et al.
American Journal of Medical Genetics. Part A|January 19, 2022
The utility of DNA methylation signatures in directing genome sequencing workflow: Kabuki syndrome and CDK13-related disorderAshish Marwaha, Gregory Costain, Cheryl Cytrynbaum, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|November 20, 2024
Infant with Refractory Seizures and Characteristic Diffusion Restriction Pattern on NeuroimagingSangeetha Yoganathan, Pradeep Krishnan, Manohar Shroff, et al.
Frontiers in Neurology|December 9, 2014
MicroRNA Dysregulation, Gene Networks, and Risk for Schizophrenia in 22q11.2 Deletion SyndromeDaniele Merico, Gregory Costain, Nancy J Butcher, et al.
Biological Psychiatry|July 19, 2014
Copy number variable microRNAs in schizophrenia and their neurodevelopmental gene targetsWilliam Warnica, Daniele Merico, Gregory Costain, et al.
Pageof 15

Showing results (41-50 of 144) with videos related to

Sort By:
Pageof 15
European Journal of Human Genetics : EJHG|September 6, 2022
Developmental implications of genetic testing for physical indicationsDanielle A Baribeau, Ny Hoang, Thanuja Selvanayagam, et al.
Seizure|October 5, 2023
Drug-resistant focal epilepsy in a girl with SETD5-related intellectual disabilityRanjith Kumar Manokaran, Ayako Ochi, Elizabeth Kerr, et al.
European Journal of Human Genetics : EJHG|November 27, 2023
Estimating the proportion of nonsense variants undergoing the newly described phenomenon of manufactured splice rescueBushra Haque, David Cheerie, Saba Birkadze, et al.
International Journal of Cardiology|December 15, 2015
Genome-wide rare copy number variations contribute to genetic risk for transposition of the great arteriesGregory Costain, Anath C Lionel, Lucas Ogura, et al.
Schizophrenia Bulletin|December 14, 2012
Evaluating genetic counseling for individuals with schizophrenia in the molecular ageGregory Costain, Mary Jane Esplen, Brenda Toner, et al.
Molecular Genetics and Metabolism Reports|November 22, 2017
Enzyme replacement therapy in perinatal hypophosphatasia: Case report of a negative outcome and lessons for clinical practiceGregory Costain, Aideen M Moore, Lauren Munroe, et al.
American Journal of Medical Genetics. Part A|January 19, 2022
The utility of DNA methylation signatures in directing genome sequencing workflow: Kabuki syndrome and CDK13-related disorderAshish Marwaha, Gregory Costain, Cheryl Cytrynbaum, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|November 20, 2024
Infant with Refractory Seizures and Characteristic Diffusion Restriction Pattern on NeuroimagingSangeetha Yoganathan, Pradeep Krishnan, Manohar Shroff, et al.
Frontiers in Neurology|December 9, 2014
MicroRNA Dysregulation, Gene Networks, and Risk for Schizophrenia in 22q11.2 Deletion SyndromeDaniele Merico, Gregory Costain, Nancy J Butcher, et al.
Biological Psychiatry|July 19, 2014
Copy number variable microRNAs in schizophrenia and their neurodevelopmental gene targetsWilliam Warnica, Daniele Merico, Gregory Costain, et al.
Pageof 15