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W Scherer

Showing results (301-310 of 915) with videos related to

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Bioinformatics (Oxford, England)|October 4, 2019
VikNGS: a C++ variant integration kit for next generation sequencing association analysisZeynep Baskurt, Scott Mastromatteo, Jiafen Gong, et al.
Genomics|November 15, 2001
Identification of the human cortactin-binding protein-2 gene from the autism candidate region at 7q31J Cheung, E Petek, K Nakabayashi, et al.
Pediatric Research|June 18, 2009
Whole genome scanning: resolving clinical diagnosis and management amidst complex dataSarah E Ali-Khan, Abdallah S Daar, Cheryl Shuman, et al.
BMC Medical Genomics|March 19, 2015
Performance of case-control rare copy number variation annotation in classification of autismWorrawat Engchuan, Kiret Dhindsa, Anath C Lionel, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 8, 1999
p200 ARF-GEP1: a Golgi-localized guanine nucleotide exchange protein whose Sec7 domain is targeted by the drug brefeldin AS J Mansour, J Skaug, X H Zhao, et al.
Research Evaluation|October 17, 2022
Evaluating the Revised National Institutes of Health Clinical Trial Definition Impact on Recruitment ProgressEugene I Kane, Gail L Daumit, Kevin M Fain, et al.
Clinical Genetics|September 7, 2005
Holoprosencephaly and cleidocranial dysplasia in a patient due to two position-effect mutations: case report and review of the literatureB A Fernandez, J Siegel-Bartelt, J-A S Herbrick, et al.
DNA Research : an International Journal for Rapid Publication of Reports on Genes and Genomes|November 5, 1998
Clustering of human chromosome fragments on the mouse genome by chromosome-mediated gene transferH Ogino, K Nakabayashi, E Michishita, et al.
Cytogenetics and Cell Genetics|January 1, 1994
Refined localization of the asparagine synthetase gene (ASNS) to chromosome 7, region q21.3, and characterization of the somatic cell hybrid line 4AF/106/KO15H H Heng, X M Shi, S W Scherer, et al.
Genes|December 23, 2023
Complex Autism Spectrum Disorder in a Patient with a Novel De Novo Heterozygous <i>MYT1L</i> VariantSilas Yip, Kristina Calli, Ying Qiao, et al.
Pageof 92

Showing results (301-310 of 915) with videos related to

Sort By:
Pageof 92
Bioinformatics (Oxford, England)|October 4, 2019
VikNGS: a C++ variant integration kit for next generation sequencing association analysisZeynep Baskurt, Scott Mastromatteo, Jiafen Gong, et al.
Genomics|November 15, 2001
Identification of the human cortactin-binding protein-2 gene from the autism candidate region at 7q31J Cheung, E Petek, K Nakabayashi, et al.
Pediatric Research|June 18, 2009
Whole genome scanning: resolving clinical diagnosis and management amidst complex dataSarah E Ali-Khan, Abdallah S Daar, Cheryl Shuman, et al.
BMC Medical Genomics|March 19, 2015
Performance of case-control rare copy number variation annotation in classification of autismWorrawat Engchuan, Kiret Dhindsa, Anath C Lionel, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 8, 1999
p200 ARF-GEP1: a Golgi-localized guanine nucleotide exchange protein whose Sec7 domain is targeted by the drug brefeldin AS J Mansour, J Skaug, X H Zhao, et al.
Research Evaluation|October 17, 2022
Evaluating the Revised National Institutes of Health Clinical Trial Definition Impact on Recruitment ProgressEugene I Kane, Gail L Daumit, Kevin M Fain, et al.
Clinical Genetics|September 7, 2005
Holoprosencephaly and cleidocranial dysplasia in a patient due to two position-effect mutations: case report and review of the literatureB A Fernandez, J Siegel-Bartelt, J-A S Herbrick, et al.
DNA Research : an International Journal for Rapid Publication of Reports on Genes and Genomes|November 5, 1998
Clustering of human chromosome fragments on the mouse genome by chromosome-mediated gene transferH Ogino, K Nakabayashi, E Michishita, et al.
Cytogenetics and Cell Genetics|January 1, 1994
Refined localization of the asparagine synthetase gene (ASNS) to chromosome 7, region q21.3, and characterization of the somatic cell hybrid line 4AF/106/KO15H H Heng, X M Shi, S W Scherer, et al.
Genes|December 23, 2023
Complex Autism Spectrum Disorder in a Patient with a Novel De Novo Heterozygous <i>MYT1L</i> VariantSilas Yip, Kristina Calli, Ying Qiao, et al.
Pageof 92