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Stuart Schwartz

Showing results (61-70 of 73) with videos related to

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Plos Genetics|January 24, 2009
Copy number variation of CCL3-like genes affects rate of progression to simian-AIDS in Rhesus Macaques (Macaca mulatta)Jeremiah D Degenhardt, Paola de Candia, Adrien Chabot, et al.
American Journal of Medical Genetics. Part A|March 16, 2013
Three cases of isolated terminal deletion of chromosome 8p without heart defects presenting with a mild phenotypeRachel D Burnside, John G Pappas, Stephanie Sacharow, et al.
Neuro-Oncology Advances|January 4, 2021
Near haploidization is a genomic hallmark which defines a molecular subgroup of giant cell glioblastomaTiffany G Baker, Jay Alden, Adrian M Dubuc, et al.
American Journal of Human Genetics|May 27, 2005
Segmental duplications and copy-number variation in the human genomeAndrew J Sharp, Devin P Locke, Sean D McGrath, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 18, 2016
Commentary on the decision of the American Board of Medical Genetics and Genomics to create a 24-month specialty of Laboratory Genetics and GenomicsFrederick R Bieber, Athena M Cherry, Beverly S Emanuel, et al.
Nature|August 20, 2004
The structure and evolution of centromeric transition regions within the human genomeXinwei She, Julie E Horvath, Zhaoshi Jiang, et al.
Human Genetics|March 2, 2011
Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delayRachel D Burnside, Romela Pasion, Fady M Mikhail, et al.
Nature Genetics|August 15, 2006
Discovery of previously unidentified genomic disorders from the duplication architecture of the human genomeAndrew J Sharp, Sierra Hansen, Rebecca R Selzer, et al.
European Journal of Human Genetics : EJHG|May 2, 2013
Reciprocal deletion and duplication at 2q23.1 indicates a role for MBD5 in autism spectrum disorderSureni V Mullegama, Jill A Rosenfeld, Carmen Orellana, et al.
American Journal of Human Genetics|December 11, 2012
Disruption of a large intergenic noncoding RNA in subjects with neurodevelopmental disabilitiesMichael E Talkowski, Gilles Maussion, Liam Crapper, et al.
Pageof 8

Showing results (61-70 of 73) with videos related to

Sort By:
Pageof 8
Plos Genetics|January 24, 2009
Copy number variation of CCL3-like genes affects rate of progression to simian-AIDS in Rhesus Macaques (Macaca mulatta)Jeremiah D Degenhardt, Paola de Candia, Adrien Chabot, et al.
American Journal of Medical Genetics. Part A|March 16, 2013
Three cases of isolated terminal deletion of chromosome 8p without heart defects presenting with a mild phenotypeRachel D Burnside, John G Pappas, Stephanie Sacharow, et al.
Neuro-Oncology Advances|January 4, 2021
Near haploidization is a genomic hallmark which defines a molecular subgroup of giant cell glioblastomaTiffany G Baker, Jay Alden, Adrian M Dubuc, et al.
American Journal of Human Genetics|May 27, 2005
Segmental duplications and copy-number variation in the human genomeAndrew J Sharp, Devin P Locke, Sean D McGrath, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 18, 2016
Commentary on the decision of the American Board of Medical Genetics and Genomics to create a 24-month specialty of Laboratory Genetics and GenomicsFrederick R Bieber, Athena M Cherry, Beverly S Emanuel, et al.
Nature|August 20, 2004
The structure and evolution of centromeric transition regions within the human genomeXinwei She, Julie E Horvath, Zhaoshi Jiang, et al.
Human Genetics|March 2, 2011
Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delayRachel D Burnside, Romela Pasion, Fady M Mikhail, et al.
Nature Genetics|August 15, 2006
Discovery of previously unidentified genomic disorders from the duplication architecture of the human genomeAndrew J Sharp, Sierra Hansen, Rebecca R Selzer, et al.
European Journal of Human Genetics : EJHG|May 2, 2013
Reciprocal deletion and duplication at 2q23.1 indicates a role for MBD5 in autism spectrum disorderSureni V Mullegama, Jill A Rosenfeld, Carmen Orellana, et al.
American Journal of Human Genetics|December 11, 2012
Disruption of a large intergenic noncoding RNA in subjects with neurodevelopmental disabilitiesMichael E Talkowski, Gilles Maussion, Liam Crapper, et al.
Pageof 8