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Showing results (511-520 of 915) with videos related to

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Scientific Reports|September 16, 2024
Chromosomal-level reference genome assembly of muskox (Ovibos moschatus) from Banks Island in the Canadian Arctic, a resource for conservation genomicsSi Lok, Timothy N H Lau, Brett Trost, et al.
American Journal of Medical Genetics. Part A|February 14, 2006
Speech and language impairment and oromotor dyspraxia due to deletion of 7q31 that involves FOXP2Susan Zeesman, Małgorzata J M Nowaczyk, Ikuko Teshima, et al.
American Journal of Human Genetics|November 14, 2007
Contribution of SHANK3 mutations to autism spectrum disorderRainald Moessner, Christian R Marshall, James S Sutcliffe, et al.
Journal of Medical Genetics|June 8, 2023
The Phenotypic variability of 16p11.2 distal BP2-BP3 deletion in a transgenerational family and in neurodevelopmentally ascertained samplesMarc Woodbury-Smith, Lia D'Abate, Dimitri J Stavropoulos, et al.
Neurology|February 4, 2011
Mitochondrial DNA haplogroups and mutations in children with acquired central demyelinationS Venkateswaran, K Zheng, M Sacchetti, et al.
Plos One|April 22, 2017
Whole-genome sequencing suggests mechanisms for 22q11.2 deletion-associated Parkinson's diseaseNancy J Butcher, Daniele Merico, Mehdi Zarrei, et al.
BMC Genomics|April 5, 2007
Human sterile alpha motif domain 9, a novel gene identified as down-regulated in aggressive fibromatosis, is absent in the mouseCatherine F Li, Jeffrey R MacDonald, Robert Y Wei, et al.
Journal of Medical Genetics|August 5, 2016
Copy-number variations are enriched for neurodevelopmental genes in children with developmental coordination disorderStephen J Mosca, Lisa Marie Langevin, Deborah Dewey, et al.
Cytogenetics and Cell Genetics|March 11, 1999
Analysis of the monomeric alphoid sequences in the pericentromeric region of human chromosome 7A de la Puente, E Velasco, L A Pérez Jurado, et al.
Genomics|January 16, 1999
A yeast artificial chromosome-based physical map of the juvenile amyotrophic lateral sclerosis (ALS2) critical region on human chromosome 2q33-q34S Hadano, K Nichol, R R Brinkman, et al.
Pageof 92

Showing results (511-520 of 915) with videos related to

Sort By:
Pageof 92
Scientific Reports|September 16, 2024
Chromosomal-level reference genome assembly of muskox (Ovibos moschatus) from Banks Island in the Canadian Arctic, a resource for conservation genomicsSi Lok, Timothy N H Lau, Brett Trost, et al.
American Journal of Medical Genetics. Part A|February 14, 2006
Speech and language impairment and oromotor dyspraxia due to deletion of 7q31 that involves FOXP2Susan Zeesman, Małgorzata J M Nowaczyk, Ikuko Teshima, et al.
American Journal of Human Genetics|November 14, 2007
Contribution of SHANK3 mutations to autism spectrum disorderRainald Moessner, Christian R Marshall, James S Sutcliffe, et al.
Journal of Medical Genetics|June 8, 2023
The Phenotypic variability of 16p11.2 distal BP2-BP3 deletion in a transgenerational family and in neurodevelopmentally ascertained samplesMarc Woodbury-Smith, Lia D'Abate, Dimitri J Stavropoulos, et al.
Neurology|February 4, 2011
Mitochondrial DNA haplogroups and mutations in children with acquired central demyelinationS Venkateswaran, K Zheng, M Sacchetti, et al.
Plos One|April 22, 2017
Whole-genome sequencing suggests mechanisms for 22q11.2 deletion-associated Parkinson's diseaseNancy J Butcher, Daniele Merico, Mehdi Zarrei, et al.
BMC Genomics|April 5, 2007
Human sterile alpha motif domain 9, a novel gene identified as down-regulated in aggressive fibromatosis, is absent in the mouseCatherine F Li, Jeffrey R MacDonald, Robert Y Wei, et al.
Journal of Medical Genetics|August 5, 2016
Copy-number variations are enriched for neurodevelopmental genes in children with developmental coordination disorderStephen J Mosca, Lisa Marie Langevin, Deborah Dewey, et al.
Cytogenetics and Cell Genetics|March 11, 1999
Analysis of the monomeric alphoid sequences in the pericentromeric region of human chromosome 7A de la Puente, E Velasco, L A Pérez Jurado, et al.
Genomics|January 16, 1999
A yeast artificial chromosome-based physical map of the juvenile amyotrophic lateral sclerosis (ALS2) critical region on human chromosome 2q33-q34S Hadano, K Nichol, R R Brinkman, et al.
Pageof 92