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W Scherer

Showing results (471-480 of 915) with videos related to

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American Journal of Nephrology|June 2, 2007
Cigarette smoking and incident chronic kidney disease: a systematic reviewCharlotte Jones-Burton, Stephen L Seliger, Roberta W Scherer, et al.
Human Molecular Genetics|April 18, 1998
Detection of a homozygous four base pair deletion in the protein X gene in a case of pyruvate dehydrogenase complex deficiencyM Ling, G McEachern, A Seyda, et al.
Plos One|March 2, 2016
Rare Copy Number Variants Identified Suggest the Regulating Pathways in Hypertension-Related Left Ventricular HypertrophyHoh Boon-Peng, Julia Ashazila Mat Jusoh, Christian R Marshall, et al.
Physical Review Letters|May 21, 2021
Cooperative Cluster Jahn-Teller Effect as a Possible Route to AntiferroelectricityK Geirhos, J Langmann, L Prodan, et al.
Oncogene|April 13, 2004
Failure of a medulloblastoma-derived mutant of SUFU to suppress WNT signalingMichael D Taylor, Xiaoyun Zhang, Ling Liu, et al.
European Journal of Medical Genetics|June 22, 2011
Phenotypic spectrum associated with duplication of Xp11.22-p11.23 includes Autism Spectrum DisorderBrian H Y Chung, Irene Drmic, Christian R Marshall, et al.
American Journal of Human Genetics|July 1, 1994
Fine mapping of the autosomal dominant split hand/split foot locus on chromosome 7, band q21.3-q22.1S W Scherer, P Poorkaj, T Allen, et al.
American Journal of Medical Genetics. Part A|August 26, 2017
De novo pathogenic variant in TUBB2A presenting with arthrogryposis multiplex congenita, brain abnormalities, and severe developmental delayResham Ejaz, Anath C Lionel, Susan Blaser, et al.
Ophthalmology|May 20, 2008
Visual fields at follow-up in the Ischemic Optic Neuropathy Decompression Trial: evaluation of change in pattern defect and severity over timeRoberta W Scherer, Steven E Feldon, Lori Levin, et al.
Data in Brief|July 25, 2019
Genome-wide copy number variant data for inflammatory bowel disease in a caucasian populationSvetlana Frenkel, Charles N Bernstein, Yong Won Jin, et al.
Pageof 92

Showing results (471-480 of 915) with videos related to

Sort By:
Pageof 92
American Journal of Nephrology|June 2, 2007
Cigarette smoking and incident chronic kidney disease: a systematic reviewCharlotte Jones-Burton, Stephen L Seliger, Roberta W Scherer, et al.
Human Molecular Genetics|April 18, 1998
Detection of a homozygous four base pair deletion in the protein X gene in a case of pyruvate dehydrogenase complex deficiencyM Ling, G McEachern, A Seyda, et al.
Plos One|March 2, 2016
Rare Copy Number Variants Identified Suggest the Regulating Pathways in Hypertension-Related Left Ventricular HypertrophyHoh Boon-Peng, Julia Ashazila Mat Jusoh, Christian R Marshall, et al.
Physical Review Letters|May 21, 2021
Cooperative Cluster Jahn-Teller Effect as a Possible Route to AntiferroelectricityK Geirhos, J Langmann, L Prodan, et al.
Oncogene|April 13, 2004
Failure of a medulloblastoma-derived mutant of SUFU to suppress WNT signalingMichael D Taylor, Xiaoyun Zhang, Ling Liu, et al.
European Journal of Medical Genetics|June 22, 2011
Phenotypic spectrum associated with duplication of Xp11.22-p11.23 includes Autism Spectrum DisorderBrian H Y Chung, Irene Drmic, Christian R Marshall, et al.
American Journal of Human Genetics|July 1, 1994
Fine mapping of the autosomal dominant split hand/split foot locus on chromosome 7, band q21.3-q22.1S W Scherer, P Poorkaj, T Allen, et al.
American Journal of Medical Genetics. Part A|August 26, 2017
De novo pathogenic variant in TUBB2A presenting with arthrogryposis multiplex congenita, brain abnormalities, and severe developmental delayResham Ejaz, Anath C Lionel, Susan Blaser, et al.
Ophthalmology|May 20, 2008
Visual fields at follow-up in the Ischemic Optic Neuropathy Decompression Trial: evaluation of change in pattern defect and severity over timeRoberta W Scherer, Steven E Feldon, Lori Levin, et al.
Data in Brief|July 25, 2019
Genome-wide copy number variant data for inflammatory bowel disease in a caucasian populationSvetlana Frenkel, Charles N Bernstein, Yong Won Jin, et al.
Pageof 92