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Gregory Costain

Showing results (31-40 of 144) with videos related to

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Circulation. Cardiovascular Genetics|February 25, 2014
Reproductive fitness and genetic transmission of tetralogy of Fallot in the molecular ageNicolas J Chin-Yee, Gregory Costain, Jodi-Ann Swaby, et al.
Journal of Medical Genetics|March 20, 2024
A comparative medical genomics approach may facilitate the interpretation of rare missense variationBushra Haque, George Guirguis, Meredith Curtis, et al.
International Journal of Cardiology|July 6, 2010
13q13.1-q13.2 deletion in tetralogy of Fallot: clinical report and a literature reviewGregory Costain, Candice K Silversides, Christian R Marshall, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 30, 2012
Functional outcomes of adults with 22q11.2 deletion syndromeNancy J Butcher, Eva W C Chow, Gregory Costain, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 19, 2015
Fetal growth and gestational factors as predictors of schizophrenia in 22q11.2 deletion syndromeLily Van, Nancy J Butcher, Gregory Costain, et al.
Journal of Genetic Counseling|January 13, 2015
Reproductive Health Issues for Adults with a Common Genomic Disorder: 22q11.2 Deletion SyndromeChrystal Chan, Gregory Costain, Lucas Ogura, et al.
Molecular Genetics and Metabolism Reports|October 26, 2020
Genome sequencing identifies a rare case of moderate Zellweger spectrum disorder caused by a <i>PEX3</i> defect: Case report and literature reviewWhiwon Lee, Gregory Costain, Susan Blaser, et al.
Brain : a Journal of Neurology|June 28, 2019
Reply: IREB2-associated neurodegenerationNunziata Maio, Manik C Ghosh, Gregory Costain, et al.
Archives of Disease in Childhood|January 4, 2023
Contemporary aetiologies of medical complexity in children: a cohort studyBushra Haque, Tayyaba Khan, Inna Ushcatz, et al.
Brain : a Journal of Neurology|March 28, 2019
Absence of iron-responsive element-binding protein 2 causes a novel neurodegenerative syndromeGregory Costain, Manik C Ghosh, Nunziata Maio, et al.
Pageof 15

Showing results (31-40 of 144) with videos related to

Sort By:
Pageof 15
Circulation. Cardiovascular Genetics|February 25, 2014
Reproductive fitness and genetic transmission of tetralogy of Fallot in the molecular ageNicolas J Chin-Yee, Gregory Costain, Jodi-Ann Swaby, et al.
Journal of Medical Genetics|March 20, 2024
A comparative medical genomics approach may facilitate the interpretation of rare missense variationBushra Haque, George Guirguis, Meredith Curtis, et al.
International Journal of Cardiology|July 6, 2010
13q13.1-q13.2 deletion in tetralogy of Fallot: clinical report and a literature reviewGregory Costain, Candice K Silversides, Christian R Marshall, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 30, 2012
Functional outcomes of adults with 22q11.2 deletion syndromeNancy J Butcher, Eva W C Chow, Gregory Costain, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 19, 2015
Fetal growth and gestational factors as predictors of schizophrenia in 22q11.2 deletion syndromeLily Van, Nancy J Butcher, Gregory Costain, et al.
Journal of Genetic Counseling|January 13, 2015
Reproductive Health Issues for Adults with a Common Genomic Disorder: 22q11.2 Deletion SyndromeChrystal Chan, Gregory Costain, Lucas Ogura, et al.
Molecular Genetics and Metabolism Reports|October 26, 2020
Genome sequencing identifies a rare case of moderate Zellweger spectrum disorder caused by a <i>PEX3</i> defect: Case report and literature reviewWhiwon Lee, Gregory Costain, Susan Blaser, et al.
Brain : a Journal of Neurology|June 28, 2019
Reply: IREB2-associated neurodegenerationNunziata Maio, Manik C Ghosh, Gregory Costain, et al.
Archives of Disease in Childhood|January 4, 2023
Contemporary aetiologies of medical complexity in children: a cohort studyBushra Haque, Tayyaba Khan, Inna Ushcatz, et al.
Brain : a Journal of Neurology|March 28, 2019
Absence of iron-responsive element-binding protein 2 causes a novel neurodegenerative syndromeGregory Costain, Manik C Ghosh, Nunziata Maio, et al.
Pageof 15