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S W Scherer

Showing results (141-150 of 164) with videos related to

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Genomics|May 18, 1999
A physical and transcriptional map of the preaxial polydactyly locus on chromosome 7q36H C Heus, A Hing, M J van Baren, et al.
Springerplus|July 8, 2016
Ankrd11 is a chromatin regulator involved in autism that is essential for neural developmentAnastassia Voronova, Denis Gallagher, Mark Zander, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 8, 1998
Molecular characterization of a common fragile site (FRA7H) on human chromosome 7 by the cloning of a simian virus 40 integration siteD Mishmar, A Rahat, S W Scherer, et al.
Journal of Medical Genetics|August 3, 2004
Genomic imprinting of PPP1R9A encoding neurabin I in skeletal muscle and extra-embryonic tissuesK Nakabayashi, S Makino, S Minagawa, et al.
Nature Genetics|June 30, 2001
Fusion of two novel genes, RBM15 and MKL1, in the t(1;22)(p13;q13) of acute megakaryoblastic leukemiaZ Ma, S W Morris, V Valentine, et al.
Clinical Genetics|December 1, 2010
Hemizygous deletions on chromosome 1p21.3 involving the DPYD gene in individuals with autism spectrum disorderM T Carter, S M Nikkel, B A Fernandez, et al.
Clinical Epigenetics|July 18, 2019
Functional DNA methylation signatures for autism spectrum disorder genomic risk loci: 16p11.2 deletions and CHD8 variantsM T Siu, D T Butcher, A L Turinsky, et al.
Molecular Psychiatry|November 18, 2015
Psychiatric gene discoveries shape evidence on ADHD's biologyA Thapar, J Martin, E Mick, et al.
Nature Genetics|November 1, 1996
Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephalyE Belloni, M Muenke, E Roessler, et al.
Cytogenetic and Genome Research|March 17, 2009
Molecular and clinical characterization of de novo and familial cases with microduplication 3q29: guidelines for copy number variation case reportingS Goobie, J Knijnenburg, D Fitzpatrick, et al.
Pageof 17

Showing results (141-150 of 164) with videos related to

Sort By:
Pageof 17
Genomics|May 18, 1999
A physical and transcriptional map of the preaxial polydactyly locus on chromosome 7q36H C Heus, A Hing, M J van Baren, et al.
Springerplus|July 8, 2016
Ankrd11 is a chromatin regulator involved in autism that is essential for neural developmentAnastassia Voronova, Denis Gallagher, Mark Zander, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 8, 1998
Molecular characterization of a common fragile site (FRA7H) on human chromosome 7 by the cloning of a simian virus 40 integration siteD Mishmar, A Rahat, S W Scherer, et al.
Journal of Medical Genetics|August 3, 2004
Genomic imprinting of PPP1R9A encoding neurabin I in skeletal muscle and extra-embryonic tissuesK Nakabayashi, S Makino, S Minagawa, et al.
Nature Genetics|June 30, 2001
Fusion of two novel genes, RBM15 and MKL1, in the t(1;22)(p13;q13) of acute megakaryoblastic leukemiaZ Ma, S W Morris, V Valentine, et al.
Clinical Genetics|December 1, 2010
Hemizygous deletions on chromosome 1p21.3 involving the DPYD gene in individuals with autism spectrum disorderM T Carter, S M Nikkel, B A Fernandez, et al.
Clinical Epigenetics|July 18, 2019
Functional DNA methylation signatures for autism spectrum disorder genomic risk loci: 16p11.2 deletions and CHD8 variantsM T Siu, D T Butcher, A L Turinsky, et al.
Molecular Psychiatry|November 18, 2015
Psychiatric gene discoveries shape evidence on ADHD's biologyA Thapar, J Martin, E Mick, et al.
Nature Genetics|November 1, 1996
Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephalyE Belloni, M Muenke, E Roessler, et al.
Cytogenetic and Genome Research|March 17, 2009
Molecular and clinical characterization of de novo and familial cases with microduplication 3q29: guidelines for copy number variation case reportingS Goobie, J Knijnenburg, D Fitzpatrick, et al.
Pageof 17