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Warren G Sanger

Showing results (51-60 of 77) with videos related to

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International Journal of Molecular Medicine|September 6, 2007
Molecular basis of aggressive disease in chronic lymphocytic leukemia patients with 11q deletion and trisomy 12 chromosomal abnormalitiesAmit K Mittal, Ganapati V Hegde, Patricia Aoun, et al.
Journal of Pediatric Hematology/Oncology|December 11, 2013
Cytosine arabinoside and mitoxantrone followed by second allogeneic transplant for the treatment of children with refractory juvenile myelomonocytic leukemiaSachit A Patel, Don W Coulter, Alfred C Grovas, et al.
British Journal of Haematology|March 18, 2008
Cytogenetic abnormalities and clinical correlations in peripheral T-cell lymphomaMarilu Nelson, Douglas E Horsman, Dennis D Weisenburger, et al.
Cancer Genetics and Cytogenetics|August 30, 2008
Occurrence of trisomy 12, t(14;18)(q32;q21), and t(8;14)(q24.1;q11.2) in a patient with B-cell chronic lymphocytic leukemiaLai-Ching Lau, Ping Lim, Yik-Chen Lim, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|May 26, 2009
t(14;18)-negative follicular lymphomas are associated with a high frequency of BCL6 rearrangement at the alternative breakpoint regionKeni Gu, Kai Fu, Smrati Jain, et al.
Cancer Genetics|October 19, 2016
Karyotypic abnormalities associated with Epstein-Barr virus status in classical Hodgkin lymphomaNathan D Montgomery, Wilborn B Coward, Steven Johnson, et al.
American Journal of Medical Genetics. Part A|May 15, 2012
Characterization of six novel patients with MECP2 duplications due to unbalanced rearrangements of the X chromosomeJennifer N Sanmann, Danielle L Bishay, Lois J Starr, et al.
Cancer Genetics and Cytogenetics|January 11, 2007
Bulky lymphadenopathy with poor clinical outcome is associated with ATM downregulation in B-cell chronic lymphocytic leukemia patients irrespective of 11q23 deletionAvadhut D Joshi, John D Dickinson, Ganapati V Hegde, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 16, 2015
Assessing the utility of confirmatory studies following identification of large-scale genomic imbalances by microarrayJennifer N Sanmann, Diane L Pickering, Denae M Golden, et al.
British Journal of Haematology|November 10, 2009
An increased frequency of 13q deletions detected by fluorescence in situ hybridization and its impact on survival in children and adolescents with Burkitt lymphoma: results from the Children's Oncology Group study CCG-5961Marilu Nelson, Sherrie L Perkins, Bhavana J Dave, et al.
Pageof 8

Showing results (51-60 of 77) with videos related to

Sort By:
Pageof 8
International Journal of Molecular Medicine|September 6, 2007
Molecular basis of aggressive disease in chronic lymphocytic leukemia patients with 11q deletion and trisomy 12 chromosomal abnormalitiesAmit K Mittal, Ganapati V Hegde, Patricia Aoun, et al.
Journal of Pediatric Hematology/Oncology|December 11, 2013
Cytosine arabinoside and mitoxantrone followed by second allogeneic transplant for the treatment of children with refractory juvenile myelomonocytic leukemiaSachit A Patel, Don W Coulter, Alfred C Grovas, et al.
British Journal of Haematology|March 18, 2008
Cytogenetic abnormalities and clinical correlations in peripheral T-cell lymphomaMarilu Nelson, Douglas E Horsman, Dennis D Weisenburger, et al.
Cancer Genetics and Cytogenetics|August 30, 2008
Occurrence of trisomy 12, t(14;18)(q32;q21), and t(8;14)(q24.1;q11.2) in a patient with B-cell chronic lymphocytic leukemiaLai-Ching Lau, Ping Lim, Yik-Chen Lim, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|May 26, 2009
t(14;18)-negative follicular lymphomas are associated with a high frequency of BCL6 rearrangement at the alternative breakpoint regionKeni Gu, Kai Fu, Smrati Jain, et al.
Cancer Genetics|October 19, 2016
Karyotypic abnormalities associated with Epstein-Barr virus status in classical Hodgkin lymphomaNathan D Montgomery, Wilborn B Coward, Steven Johnson, et al.
American Journal of Medical Genetics. Part A|May 15, 2012
Characterization of six novel patients with MECP2 duplications due to unbalanced rearrangements of the X chromosomeJennifer N Sanmann, Danielle L Bishay, Lois J Starr, et al.
Cancer Genetics and Cytogenetics|January 11, 2007
Bulky lymphadenopathy with poor clinical outcome is associated with ATM downregulation in B-cell chronic lymphocytic leukemia patients irrespective of 11q23 deletionAvadhut D Joshi, John D Dickinson, Ganapati V Hegde, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 16, 2015
Assessing the utility of confirmatory studies following identification of large-scale genomic imbalances by microarrayJennifer N Sanmann, Diane L Pickering, Denae M Golden, et al.
British Journal of Haematology|November 10, 2009
An increased frequency of 13q deletions detected by fluorescence in situ hybridization and its impact on survival in children and adolescents with Burkitt lymphoma: results from the Children's Oncology Group study CCG-5961Marilu Nelson, Sherrie L Perkins, Bhavana J Dave, et al.
Pageof 8