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Stephen W Scherer

Showing results (31-40 of 499) with videos related to

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Epilepsy Research|August 26, 2006
Protein therapy for Unverricht-Lundborg disease using cystatin B transduction by TAT-PTD. Is it that simple?Danielle M Andrade, Stephen W Scherer, Berge A Minassian
G3 (Bethesda, Md.)|August 9, 2013
Building trust in 21st century genomicsMichael J Szego, Janet A Buchanan, Stephen W Scherer
Human Molecular Genetics|October 4, 2007
Copy-number variation in control population cohortsDalila Pinto, Christian Marshall, Lars Feuk, et al.
Biochemical and Biophysical Research Communications|January 22, 2003
A third human carnitine/organic cation transporter (OCTN3) as a candidate for the 5q31 Crohn's disease locus (IBD5)Anne-Marie Lamhonwah, Jennifer Skaug, Stephen W Scherer, et al.
Nature Reviews. Genetics|February 4, 2015
A copy number variation map of the human genomeMehdi Zarrei, Jeffrey R MacDonald, Daniele Merico, et al.
Methods in Molecular Medicine|August 26, 2006
Williams-Beuren syndrome diagnosis using fluorescence in situ hybridizationLucy R Osborne, Ann M Joseph-George, Stephen W Scherer
Biochemical and Biophysical Research Communications|October 19, 2006
IQCJ-SCHIP1, a novel fusion transcript encoding a calmodulin-binding IQ motif proteinDorota A Kwaśnicka-Crawford, Andrew R Carson, Stephen W Scherer
Human Genomics|July 20, 2006
Strategies for the detection of copy number and other structural variants in the human genomeAndrew R Carson, Lars Feuk, Mansoor Mohammed, et al.
Molecular Psychiatry|May 18, 2021
Environmental exposures associated with elevated risk for autism spectrum disorder may augment the burden of deleterious de novo mutations among probandsKealan Pugsley, Stephen W Scherer, Mark A Bellgrove, et al.
Methods in Molecular Biology (Clifton, N.J.)|August 5, 2006
Methods for identifying and mapping recent segmental and gene duplications in eukaryotic genomesRazi Khaja, Jeffrey R MacDonald, Junjun Zhang, et al.
Pageof 50

Showing results (31-40 of 499) with videos related to

Sort By:
Pageof 50
Epilepsy Research|August 26, 2006
Protein therapy for Unverricht-Lundborg disease using cystatin B transduction by TAT-PTD. Is it that simple?Danielle M Andrade, Stephen W Scherer, Berge A Minassian
G3 (Bethesda, Md.)|August 9, 2013
Building trust in 21st century genomicsMichael J Szego, Janet A Buchanan, Stephen W Scherer
Human Molecular Genetics|October 4, 2007
Copy-number variation in control population cohortsDalila Pinto, Christian Marshall, Lars Feuk, et al.
Biochemical and Biophysical Research Communications|January 22, 2003
A third human carnitine/organic cation transporter (OCTN3) as a candidate for the 5q31 Crohn's disease locus (IBD5)Anne-Marie Lamhonwah, Jennifer Skaug, Stephen W Scherer, et al.
Nature Reviews. Genetics|February 4, 2015
A copy number variation map of the human genomeMehdi Zarrei, Jeffrey R MacDonald, Daniele Merico, et al.
Methods in Molecular Medicine|August 26, 2006
Williams-Beuren syndrome diagnosis using fluorescence in situ hybridizationLucy R Osborne, Ann M Joseph-George, Stephen W Scherer
Biochemical and Biophysical Research Communications|October 19, 2006
IQCJ-SCHIP1, a novel fusion transcript encoding a calmodulin-binding IQ motif proteinDorota A Kwaśnicka-Crawford, Andrew R Carson, Stephen W Scherer
Human Genomics|July 20, 2006
Strategies for the detection of copy number and other structural variants in the human genomeAndrew R Carson, Lars Feuk, Mansoor Mohammed, et al.
Molecular Psychiatry|May 18, 2021
Environmental exposures associated with elevated risk for autism spectrum disorder may augment the burden of deleterious de novo mutations among probandsKealan Pugsley, Stephen W Scherer, Mark A Bellgrove, et al.
Methods in Molecular Biology (Clifton, N.J.)|August 5, 2006
Methods for identifying and mapping recent segmental and gene duplications in eukaryotic genomesRazi Khaja, Jeffrey R MacDonald, Junjun Zhang, et al.
Pageof 50