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Gregory Costain

Showing results (51-60 of 144) with videos related to

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Schizophrenia Research|July 20, 2010
Reduced gray matter in the anterior cingulate gyrus in familial schizophrenia: a preliminary reportGregory Costain, Andrew Ho, Adrian P Crawley, et al.
Molecular Cytogenetics|March 22, 2014
Adult expression of a 3q13.31 microdeletionChelsea Lowther, Gregory Costain, Rebecca Melvin, et al.
Journal of Pediatric Genetics|August 15, 2018
Challenges in Diagnosing Rare Genetic Causes of Common In Utero Presentations: Report of Two Patients with Mucolipidosis Type II (I-Cell Disease)Gregory Costain, Michal Inbar-Feigenberg, Maha Saleh, et al.
Journal of Medical Genetics|May 20, 2022
Gain-of-function p.F28S variant in <i>RAC3</i> disrupts neuronal differentiation, migration and axonogenesis during cortical development, leading to neurodevelopmental disorderMasashi Nishikawa, Marcello Scala, Muhammad Umair, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|July 1, 2024
Diagnostic evaluation of patients with epileptic spasms in the era of next-generation sequencingAli Mir, Mohammed AlQahtani, Fawzia Amer, et al.
Paediatrics & Child Health|October 6, 2025
Implementing a consultation service for translating genomic research findings into the clinic: Lessons from the SickKids Genome BoardAmy Y Pan, Kenzie Pulsifer, Michelle M Axford, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 9, 2014
Adult neuropsychiatric expression and familial segregation of 2q13 duplicationsGregory Costain, Anath C Lionel, Fiona Fu, et al.
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|January 19, 2025
Insights into the effects of subretinal voretigene neparvovec-rzyl in RPE65-associated Leber congenital amaurosisAlaa Tayyib, Deepika C Parameswarappa, Peter J Kertes, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 7, 2026
Interventional Genomics: Bridging Germline Diagnosis and Therapeutic ActionPetros Giannikopoulos, Marlen C Lauffer, Christian R Marshall, et al.
Psychological Medicine|January 14, 2021
Within-family influences on dimensional neurobehavioral traits in a high-risk genetic modelAnia M Fiksinski, Tracy Heung, Maria Corral, et al.
Pageof 15

Showing results (51-60 of 144) with videos related to

Sort By:
Pageof 15
Schizophrenia Research|July 20, 2010
Reduced gray matter in the anterior cingulate gyrus in familial schizophrenia: a preliminary reportGregory Costain, Andrew Ho, Adrian P Crawley, et al.
Molecular Cytogenetics|March 22, 2014
Adult expression of a 3q13.31 microdeletionChelsea Lowther, Gregory Costain, Rebecca Melvin, et al.
Journal of Pediatric Genetics|August 15, 2018
Challenges in Diagnosing Rare Genetic Causes of Common In Utero Presentations: Report of Two Patients with Mucolipidosis Type II (I-Cell Disease)Gregory Costain, Michal Inbar-Feigenberg, Maha Saleh, et al.
Journal of Medical Genetics|May 20, 2022
Gain-of-function p.F28S variant in <i>RAC3</i> disrupts neuronal differentiation, migration and axonogenesis during cortical development, leading to neurodevelopmental disorderMasashi Nishikawa, Marcello Scala, Muhammad Umair, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|July 1, 2024
Diagnostic evaluation of patients with epileptic spasms in the era of next-generation sequencingAli Mir, Mohammed AlQahtani, Fawzia Amer, et al.
Paediatrics & Child Health|October 6, 2025
Implementing a consultation service for translating genomic research findings into the clinic: Lessons from the SickKids Genome BoardAmy Y Pan, Kenzie Pulsifer, Michelle M Axford, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 9, 2014
Adult neuropsychiatric expression and familial segregation of 2q13 duplicationsGregory Costain, Anath C Lionel, Fiona Fu, et al.
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|January 19, 2025
Insights into the effects of subretinal voretigene neparvovec-rzyl in RPE65-associated Leber congenital amaurosisAlaa Tayyib, Deepika C Parameswarappa, Peter J Kertes, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 7, 2026
Interventional Genomics: Bridging Germline Diagnosis and Therapeutic ActionPetros Giannikopoulos, Marlen C Lauffer, Christian R Marshall, et al.
Psychological Medicine|January 14, 2021
Within-family influences on dimensional neurobehavioral traits in a high-risk genetic modelAnia M Fiksinski, Tracy Heung, Maria Corral, et al.
Pageof 15