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Christian R Marshall

Showing results (1-10 of 217) with videos related to

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Methods in Molecular Biology (Clifton, N.J.)|January 10, 2012
Detection and characterization of copy number variation in autism spectrum disorderChristian R Marshall, Stephen W Scherer
Prenatal Diagnosis|October 9, 2016
Neuropsychiatric aspects of 22q11.2 deletion syndrome: considerations in the prenatal settingAnne S Bassett, Gregory Costain, Christian R Marshall
Physiological Genomics|October 18, 2007
Functional and evolutionary relationships of troponin CTodd E Gillis, Christian R Marshall, Glen F Tibbits
Physiological Genomics|January 18, 2007
Evolution and structural diversification of hyperpolarization-activated cyclic nucleotide-gated channel genesHeather A Jackson, Christian R Marshall, Eric A Accili
Human Molecular Genetics|May 3, 2006
Structural variants: changing the landscape of chromosomes and design of disease studiesLars Feuk, Christian R Marshall, Richard F Wintle, et al.
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|October 26, 2021
Genome sequencing as a diagnostic testGregory Costain, Ronald D Cohn, Stephen W Scherer, et al.
European Journal of Human Genetics : EJHG|April 6, 2017
Severe neurodegeneration, progressive cerebral volume loss and diffuse hypomyelination associated with a homozygous frameshift mutation in CSTBAlan O'Brien, Christian R Marshall, Susan Blaser, et al.
BMC Evolutionary Biology|May 2, 2008
Gene structure evolution of the Na+-Ca2+ exchanger (NCX) familyCaly On, Christian R Marshall, Nansheng Chen, et al.
Human Mutation|May 29, 2016
Arginine-Glycine Amidinotransferase Deficiency and Functional Characterization of Missense Variants in GATMCaro-Lyne DesRoches, Theodora Bruun, Peixiang Wang, et al.
American Journal of Medical Genetics. Part A|June 18, 2016
MED23-associated refractory epilepsy successfully treated with the ketogenic dietAnath C Lionel, Nasim Monfared, Stephen W Scherer, et al.
Pageof 22

Showing results (1-10 of 217) with videos related to

Sort By:
Pageof 22
Methods in Molecular Biology (Clifton, N.J.)|January 10, 2012
Detection and characterization of copy number variation in autism spectrum disorderChristian R Marshall, Stephen W Scherer
Prenatal Diagnosis|October 9, 2016
Neuropsychiatric aspects of 22q11.2 deletion syndrome: considerations in the prenatal settingAnne S Bassett, Gregory Costain, Christian R Marshall
Physiological Genomics|October 18, 2007
Functional and evolutionary relationships of troponin CTodd E Gillis, Christian R Marshall, Glen F Tibbits
Physiological Genomics|January 18, 2007
Evolution and structural diversification of hyperpolarization-activated cyclic nucleotide-gated channel genesHeather A Jackson, Christian R Marshall, Eric A Accili
Human Molecular Genetics|May 3, 2006
Structural variants: changing the landscape of chromosomes and design of disease studiesLars Feuk, Christian R Marshall, Richard F Wintle, et al.
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|October 26, 2021
Genome sequencing as a diagnostic testGregory Costain, Ronald D Cohn, Stephen W Scherer, et al.
European Journal of Human Genetics : EJHG|April 6, 2017
Severe neurodegeneration, progressive cerebral volume loss and diffuse hypomyelination associated with a homozygous frameshift mutation in CSTBAlan O'Brien, Christian R Marshall, Susan Blaser, et al.
BMC Evolutionary Biology|May 2, 2008
Gene structure evolution of the Na+-Ca2+ exchanger (NCX) familyCaly On, Christian R Marshall, Nansheng Chen, et al.
Human Mutation|May 29, 2016
Arginine-Glycine Amidinotransferase Deficiency and Functional Characterization of Missense Variants in GATMCaro-Lyne DesRoches, Theodora Bruun, Peixiang Wang, et al.
American Journal of Medical Genetics. Part A|June 18, 2016
MED23-associated refractory epilepsy successfully treated with the ketogenic dietAnath C Lionel, Nasim Monfared, Stephen W Scherer, et al.
Pageof 22