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Christian Marshall

Showing results (11-20 of 21) with videos related to

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Psychiatric Genetics|May 23, 2008
A translocation t(6;7)(p11-p12;q22) associated with autism and mental retardation: localization and identification of candidate genes at the breakpointsJohn B Vincent, Sanaa Choufani, Shin-ichi Horike, et al.
American Journal of Human Genetics|January 8, 2013
Metaphyseal dysplasia with maxillary hypoplasia and brachydactyly is caused by a duplication in RUNX2Pierre Moffatt, Mouna Ben Amor, Francis H Glorieux, et al.
American Journal of Human Genetics|November 22, 2016
Epileptic Encephalopathy Caused by Mutations in the Guanine Nucleotide Exchange Factor DENND5AChanshuai Han, Reem Alkhater, Tawfiq Froukh, et al.
American Journal of Human Genetics|June 7, 2014
FORGE Canada Consortium: outcomes of a 2-year national rare-disease gene-discovery projectChandree L Beaulieu, Jacek Majewski, Jeremy Schwartzentruber, et al.
Plos Genetics|September 13, 2012
Rare copy number variants contribute to congenital left-sided heart diseaseMarc-Phillip Hitz, Louis-Philippe Lemieux-Perreault, Christian Marshall, et al.
BMJ Open|September 4, 2024
Genetics Navigator: protocol for a mixed methods randomized controlled trial evaluating a digital platform to deliver genomic services in Canadian pediatric and adult populationsGuylaine D'Amours, Marc Clausen, Stephanie Luca, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 26, 2025
Mainstreaming of clinical genetic testing: A conceptual frameworkMichael P Mackley, Julie Richer, Andrea Guerin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 13, 2016
Recommendations for the integration of genomics into clinical practiceSarah Bowdin, Adel Gilbert, Emma Bedoukian, et al.
Journal of the American Academy of Child and Adolescent Psychiatry|July 27, 2014
Copy number variation in obsessive-compulsive disorder and tourette syndrome: a cross-disorder studyLauren M McGrath, Dongmei Yu, Christian Marshall, et al.
Molecular Psychiatry|February 5, 2020
Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletionIsabelle Cleynen, Worrawat Engchuan, Matthew S Hestand, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Psychiatric Genetics|May 23, 2008
A translocation t(6;7)(p11-p12;q22) associated with autism and mental retardation: localization and identification of candidate genes at the breakpointsJohn B Vincent, Sanaa Choufani, Shin-ichi Horike, et al.
American Journal of Human Genetics|January 8, 2013
Metaphyseal dysplasia with maxillary hypoplasia and brachydactyly is caused by a duplication in RUNX2Pierre Moffatt, Mouna Ben Amor, Francis H Glorieux, et al.
American Journal of Human Genetics|November 22, 2016
Epileptic Encephalopathy Caused by Mutations in the Guanine Nucleotide Exchange Factor DENND5AChanshuai Han, Reem Alkhater, Tawfiq Froukh, et al.
American Journal of Human Genetics|June 7, 2014
FORGE Canada Consortium: outcomes of a 2-year national rare-disease gene-discovery projectChandree L Beaulieu, Jacek Majewski, Jeremy Schwartzentruber, et al.
Plos Genetics|September 13, 2012
Rare copy number variants contribute to congenital left-sided heart diseaseMarc-Phillip Hitz, Louis-Philippe Lemieux-Perreault, Christian Marshall, et al.
BMJ Open|September 4, 2024
Genetics Navigator: protocol for a mixed methods randomized controlled trial evaluating a digital platform to deliver genomic services in Canadian pediatric and adult populationsGuylaine D'Amours, Marc Clausen, Stephanie Luca, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 26, 2025
Mainstreaming of clinical genetic testing: A conceptual frameworkMichael P Mackley, Julie Richer, Andrea Guerin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 13, 2016
Recommendations for the integration of genomics into clinical practiceSarah Bowdin, Adel Gilbert, Emma Bedoukian, et al.
Journal of the American Academy of Child and Adolescent Psychiatry|July 27, 2014
Copy number variation in obsessive-compulsive disorder and tourette syndrome: a cross-disorder studyLauren M McGrath, Dongmei Yu, Christian Marshall, et al.
Molecular Psychiatry|February 5, 2020
Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletionIsabelle Cleynen, Worrawat Engchuan, Matthew S Hestand, et al.
Pageof 3