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Showing results (391-400 of 915) with videos related to

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Journal of Physics. Condensed Matter : an Institute of Physics Journal|March 28, 2015
On the nature of superconductivity in the anisotropic dichalcogenide NbSe2{CoCp2}xE-W Scheidt, M Herzinger, A Fischer, et al.
American Journal of Medical Genetics. Part A|April 9, 2015
De novo exon 1 deletion of AUTS2 gene in a patient with autism spectrum disorder and developmental delay: a case report and a brief literature reviewYi Liu, Dongmei Zhao, Rui Dong, et al.
Genome Research|October 29, 2024
Resolving complex duplication variants in autism spectrum disorder using long-read genome sequencingJesper Eisfeldt, Edward J Higginbotham, Felix Lenner, et al.
Human Mutation|April 23, 2009
Genomic variation in a global village: report of the 10th annual Human Genome Variation Meeting 2008Anthony J Brookes, Stephen J Chanock, Thomas J Hudson, et al.
Journal of Cellular and Molecular Medicine|July 30, 2008
Abnormal connexin43 in arrhythmogenic right ventricular cardiomyopathy caused by plakophilin-2 mutationsLee M Fidler, Gregory J Wilson, Fanfan Liu, et al.
Genomics|March 21, 1998
The hyaluronidase gene HYAL1 maps to chromosome 3p21.2-p21.3 in human and 9F1-F2 in mouse, a conserved candidate tumor suppressor locusA B Csóka, G I Frost, H H Heng, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 30, 2015
Rare de novo deletion of metabotropic glutamate receptor 7 (GRM7) gene in a patient with autism spectrum disorderYi Liu, Yanqing Zhang, Dongmei Zhao, et al.
Genomics|December 28, 1999
Genomic structure of the adult-onset type II citrullinemia gene, SLC25A13, and cloning and expression of its mouse homologueD S Sinasac, M A Crackower, J R Lee, et al.
Annals of Neurology|February 28, 2001
Laforin is a cell membrane and endoplasmic reticulum-associated protein tyrosine phosphataseB A Minassian, D M Andrade, L Ianzano, et al.
Plos Genetics|October 29, 2005
Discovery of human inversion polymorphisms by comparative analysis of human and chimpanzee DNA sequence assembliesLars Feuk, Jeffrey R MacDonald, Terence Tang, et al.
Pageof 92

Showing results (391-400 of 915) with videos related to

Sort By:
Pageof 92
Journal of Physics. Condensed Matter : an Institute of Physics Journal|March 28, 2015
On the nature of superconductivity in the anisotropic dichalcogenide NbSe2{CoCp2}xE-W Scheidt, M Herzinger, A Fischer, et al.
American Journal of Medical Genetics. Part A|April 9, 2015
De novo exon 1 deletion of AUTS2 gene in a patient with autism spectrum disorder and developmental delay: a case report and a brief literature reviewYi Liu, Dongmei Zhao, Rui Dong, et al.
Genome Research|October 29, 2024
Resolving complex duplication variants in autism spectrum disorder using long-read genome sequencingJesper Eisfeldt, Edward J Higginbotham, Felix Lenner, et al.
Human Mutation|April 23, 2009
Genomic variation in a global village: report of the 10th annual Human Genome Variation Meeting 2008Anthony J Brookes, Stephen J Chanock, Thomas J Hudson, et al.
Journal of Cellular and Molecular Medicine|July 30, 2008
Abnormal connexin43 in arrhythmogenic right ventricular cardiomyopathy caused by plakophilin-2 mutationsLee M Fidler, Gregory J Wilson, Fanfan Liu, et al.
Genomics|March 21, 1998
The hyaluronidase gene HYAL1 maps to chromosome 3p21.2-p21.3 in human and 9F1-F2 in mouse, a conserved candidate tumor suppressor locusA B Csóka, G I Frost, H H Heng, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 30, 2015
Rare de novo deletion of metabotropic glutamate receptor 7 (GRM7) gene in a patient with autism spectrum disorderYi Liu, Yanqing Zhang, Dongmei Zhao, et al.
Genomics|December 28, 1999
Genomic structure of the adult-onset type II citrullinemia gene, SLC25A13, and cloning and expression of its mouse homologueD S Sinasac, M A Crackower, J R Lee, et al.
Annals of Neurology|February 28, 2001
Laforin is a cell membrane and endoplasmic reticulum-associated protein tyrosine phosphataseB A Minassian, D M Andrade, L Ianzano, et al.
Plos Genetics|October 29, 2005
Discovery of human inversion polymorphisms by comparative analysis of human and chimpanzee DNA sequence assembliesLars Feuk, Jeffrey R MacDonald, Terence Tang, et al.
Pageof 92