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Roger A Schultz

Showing results (11-20 of 44) with videos related to

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Genomics|February 28, 2002
Genomic organization and mapping of the gene encoding the PP2A B56gamma regulatory subunitSabeeha Muneer, Vivek Ramalingam, Robert Wyatt, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|November 10, 2007
Translocation (4;19)(q35;q13.1)-associated primitive round cell sarcoma: report of a case and review of the literatureDinesh Rakheja, Stanton Goldman, Kathleen S Wilson, et al.
DNA Repair|November 7, 2006
Validation of XP-C pathogenic variations in archival material from a live XP patientLisa D McDaniel, Amanda Rivera-Begeman, Ana T Doughty, et al.
DNA Repair|December 4, 2003
Chromosome instability and tumor predisposition inversely correlate with BLM protein levelsLisa D McDaniel, Nicholas Chester, Mark Watson, et al.
Molecular Cytogenetics|February 17, 2009
MODY-like diabetes associated with an apparently balanced translocation: possible involvement of MPP7 gene and cell polarity in the pathogenesis of diabetesElizabeth J Bhoj, Stefano Romeo, Marco G Baroni, et al.
DNA Repair|March 20, 2010
Small scale genetic alterations contribute to increased mutability at the X-linked Hprt locus in vivo in Blm hypomorphic miceIrina V Tereshchenko, Yanping Chen, Lisa D McDaniel, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|March 5, 2005
Renal metanephric adenoma with previously unreported cytogenetic abnormalities: case report and review of the literatureDinesh Rakheja, Fangru Lian, Gail E Tomlinson, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|January 5, 2005
Extrapleural benign solitary fibrous tumor in the shoulder of a 9-year-old girl: case report and review of the literatureDinesh Rakheja, Kathleen S Wilson, John J Meehan, et al.
American Journal of Human Genetics|May 12, 2005
Mapping of a single locus capable of complementing the defective heterochromatin phenotype of Roberts syndrome cellsLisa D McDaniel, Darrell J Tomkins, Eric J Stanbridge, et al.
Clinical Lymphoma, Myeloma & Leukemia|June 18, 2013
Value of oligonucleotide-based array comparative genomic hybridization for diagnosis of acute promyelocytic leukemia in a patient negative for t(15;17)(q24.1;q21.2)/promyelocytic leukemia-retinoic acid receptor, alpha by conventional cytogenetics and fluorescence in situ hybridizationKhaled Alayed, L Jeffrey Medeiros, Roger A Schultz, et al.
Pageof 5

Showing results (11-20 of 44) with videos related to

Sort By:
Pageof 5
Genomics|February 28, 2002
Genomic organization and mapping of the gene encoding the PP2A B56gamma regulatory subunitSabeeha Muneer, Vivek Ramalingam, Robert Wyatt, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|November 10, 2007
Translocation (4;19)(q35;q13.1)-associated primitive round cell sarcoma: report of a case and review of the literatureDinesh Rakheja, Stanton Goldman, Kathleen S Wilson, et al.
DNA Repair|November 7, 2006
Validation of XP-C pathogenic variations in archival material from a live XP patientLisa D McDaniel, Amanda Rivera-Begeman, Ana T Doughty, et al.
DNA Repair|December 4, 2003
Chromosome instability and tumor predisposition inversely correlate with BLM protein levelsLisa D McDaniel, Nicholas Chester, Mark Watson, et al.
Molecular Cytogenetics|February 17, 2009
MODY-like diabetes associated with an apparently balanced translocation: possible involvement of MPP7 gene and cell polarity in the pathogenesis of diabetesElizabeth J Bhoj, Stefano Romeo, Marco G Baroni, et al.
DNA Repair|March 20, 2010
Small scale genetic alterations contribute to increased mutability at the X-linked Hprt locus in vivo in Blm hypomorphic miceIrina V Tereshchenko, Yanping Chen, Lisa D McDaniel, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|March 5, 2005
Renal metanephric adenoma with previously unreported cytogenetic abnormalities: case report and review of the literatureDinesh Rakheja, Fangru Lian, Gail E Tomlinson, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|January 5, 2005
Extrapleural benign solitary fibrous tumor in the shoulder of a 9-year-old girl: case report and review of the literatureDinesh Rakheja, Kathleen S Wilson, John J Meehan, et al.
American Journal of Human Genetics|May 12, 2005
Mapping of a single locus capable of complementing the defective heterochromatin phenotype of Roberts syndrome cellsLisa D McDaniel, Darrell J Tomkins, Eric J Stanbridge, et al.
Clinical Lymphoma, Myeloma & Leukemia|June 18, 2013
Value of oligonucleotide-based array comparative genomic hybridization for diagnosis of acute promyelocytic leukemia in a patient negative for t(15;17)(q24.1;q21.2)/promyelocytic leukemia-retinoic acid receptor, alpha by conventional cytogenetics and fluorescence in situ hybridizationKhaled Alayed, L Jeffrey Medeiros, Roger A Schultz, et al.
Pageof 5