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Showing results (631-640 of 915) with videos related to

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G3 (Bethesda, Md.)|January 1, 2013
A discovery resource of rare copy number variations in individuals with autism spectrum disorderAparna Prasad, Daniele Merico, Bhooma Thiruvahindrapuram, et al.
Journal of Medical Genetics|September 14, 2019
Impact of DNA source on genetic variant detection from human whole-genome sequencing dataBrett Trost, Susan Walker, Syed A Haider, et al.
Human Genetics|July 20, 2007
Germ-line DNA copy number variation frequencies in a large North American populationGeorge Zogopoulos, Kevin C H Ha, Faisal Naqib, et al.
Genome Research|July 1, 2006
Copy number variation: new insights in genome diversityJennifer L Freeman, George H Perry, Lars Feuk, et al.
Neurology. Genetics|February 12, 2020
Critical exon indexing improves clinical interpretation of copy number variants in neurodevelopmental disordersE Robert Wassman, Karen S Ho, Diana Bertrand, et al.
Molecular Psychiatry|May 2, 2022
Mutations in trpγ, the homologue of TRPC6 autism candidate gene, causes autism-like behavioral deficits in DrosophilaAngelina Palacios-Muñoz, Danielle de Paula Moreira, Valeria Silva, et al.
Genome Biology|May 21, 2010
Towards a comprehensive structural variation map of an individual human genomeAndy W Pang, Jeffrey R MacDonald, Dalila Pinto, et al.
NPJ Genomic Medicine|November 19, 2021
Homozygous duplication identified by whole genome sequencing causes LRBA deficiencyDaniele Merico, Yehonatan Pasternak, Mehdi Zarrei, et al.
Critical Reviews in Toxicology|September 18, 2013
A survey of frameworks for best practices in weight-of-evidence analysesLorenz R Rhomberg, Julie E Goodman, Lisa A Bailey, et al.
The New England Journal of Medicine|October 21, 2005
Severe expressive-language delay related to duplication of the Williams-Beuren locusMartin J Somerville, Carolyn B Mervis, Edwin J Young, et al.
Pageof 92

Showing results (631-640 of 915) with videos related to

Sort By:
Pageof 92
G3 (Bethesda, Md.)|January 1, 2013
A discovery resource of rare copy number variations in individuals with autism spectrum disorderAparna Prasad, Daniele Merico, Bhooma Thiruvahindrapuram, et al.
Journal of Medical Genetics|September 14, 2019
Impact of DNA source on genetic variant detection from human whole-genome sequencing dataBrett Trost, Susan Walker, Syed A Haider, et al.
Human Genetics|July 20, 2007
Germ-line DNA copy number variation frequencies in a large North American populationGeorge Zogopoulos, Kevin C H Ha, Faisal Naqib, et al.
Genome Research|July 1, 2006
Copy number variation: new insights in genome diversityJennifer L Freeman, George H Perry, Lars Feuk, et al.
Neurology. Genetics|February 12, 2020
Critical exon indexing improves clinical interpretation of copy number variants in neurodevelopmental disordersE Robert Wassman, Karen S Ho, Diana Bertrand, et al.
Molecular Psychiatry|May 2, 2022
Mutations in trpγ, the homologue of TRPC6 autism candidate gene, causes autism-like behavioral deficits in DrosophilaAngelina Palacios-Muñoz, Danielle de Paula Moreira, Valeria Silva, et al.
Genome Biology|May 21, 2010
Towards a comprehensive structural variation map of an individual human genomeAndy W Pang, Jeffrey R MacDonald, Dalila Pinto, et al.
NPJ Genomic Medicine|November 19, 2021
Homozygous duplication identified by whole genome sequencing causes LRBA deficiencyDaniele Merico, Yehonatan Pasternak, Mehdi Zarrei, et al.
Critical Reviews in Toxicology|September 18, 2013
A survey of frameworks for best practices in weight-of-evidence analysesLorenz R Rhomberg, Julie E Goodman, Lisa A Bailey, et al.
The New England Journal of Medicine|October 21, 2005
Severe expressive-language delay related to duplication of the Williams-Beuren locusMartin J Somerville, Carolyn B Mervis, Edwin J Young, et al.
Pageof 92