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Stéphanie Struski

Showing results (1-10 of 23) with videos related to

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Cancer Genetics and Cytogenetics|June 20, 2002
Compilation of published comparative genomic hybridization studiesStéphanie Struski, Martine Doco-Fenzy, Pascale Cornillet-Lefebvre
Annales De Biologie Clinique|September 16, 2016
Cytogenetics in the management of chronic lymphocytic leukemia: an update by the Groupe francophone de cytogénétique hématologique (GFCH)Florence Nguyen-Khac, Claire Borie, Evelyne Callet-Bauchu, et al.
Cancer Genetics and Cytogenetics|November 27, 2007
Confirmation of a novel recurrent association: BCR-ABL t(9;22) and t(19;21)Stéphanie Struski, Catherine Hélias, Carine Gervais, et al.
Cancer Genetics and Cytogenetics|July 18, 2006
Cytogenetic studies of a series of 43 consecutive secondary myelodysplastic syndromes/acute myeloid leukemias: conventional cytogenetics, FISH, and multiplex FISHWei Shali, Catherine Hélias, Cécile Fohrer, et al.
Hematological Oncology|September 29, 2016
Major prognostic value of complex karyotype in addition to TP53 and IGHV mutational status in first-line chronic lymphocytic leukemiaYannick Le Bris, Stéphanie Struski, Romain Guièze, et al.
Analytical Cellular Pathology : the Journal of the European Society for Analytical Cellular Pathology|May 31, 2003
Cytogenetic evolution of human ovarian cell lines associated with chemoresistance and loss of tumorigenicityStéphanie Struski, Martine Doco-Fenzy, Michael Koehler, et al.
Cancer Research|August 3, 2005
AF4p12, a human homologue to the furry gene of Drosophila, as a novel MLL fusion partnerSandrine Hayette, Pascale Cornillet-Lefebvre, Isabelle Tigaud, et al.
American Journal of Medical Genetics. Part A|January 18, 2006
Pure direct duplication (12)(q24.1-->q24.2) in a child with Marcus Gunn phenomenon and multiple congenital anomaliesMartine Doco-Fenzy, Pierre Mauran, Jean Marie Lebrun, et al.
Genes, Chromosomes & Cancer|September 12, 2018
Mutational and cytogenetic analyses of 188 CLL patients with trisomy 12: A retrospective study from the French Innovative Leukemia Organization (FILO) working groupDamien Roos-Weil, Florence Nguyen-Khac, Sylvie Chevret, et al.
Leukemia Research|May 2, 2009
Gain of the short arm of chromosome 2 (2p) is a frequent recurring chromosome aberration in untreated chronic lymphocytic leukemia (CLL) at advanced stagesElise Chapiro, Nathalie Leporrier, Isabelle Radford-Weiss, et al.
Pageof 3

Showing results (1-10 of 23) with videos related to

Sort By:
Pageof 3
Cancer Genetics and Cytogenetics|June 20, 2002
Compilation of published comparative genomic hybridization studiesStéphanie Struski, Martine Doco-Fenzy, Pascale Cornillet-Lefebvre
Annales De Biologie Clinique|September 16, 2016
Cytogenetics in the management of chronic lymphocytic leukemia: an update by the Groupe francophone de cytogénétique hématologique (GFCH)Florence Nguyen-Khac, Claire Borie, Evelyne Callet-Bauchu, et al.
Cancer Genetics and Cytogenetics|November 27, 2007
Confirmation of a novel recurrent association: BCR-ABL t(9;22) and t(19;21)Stéphanie Struski, Catherine Hélias, Carine Gervais, et al.
Cancer Genetics and Cytogenetics|July 18, 2006
Cytogenetic studies of a series of 43 consecutive secondary myelodysplastic syndromes/acute myeloid leukemias: conventional cytogenetics, FISH, and multiplex FISHWei Shali, Catherine Hélias, Cécile Fohrer, et al.
Hematological Oncology|September 29, 2016
Major prognostic value of complex karyotype in addition to TP53 and IGHV mutational status in first-line chronic lymphocytic leukemiaYannick Le Bris, Stéphanie Struski, Romain Guièze, et al.
Analytical Cellular Pathology : the Journal of the European Society for Analytical Cellular Pathology|May 31, 2003
Cytogenetic evolution of human ovarian cell lines associated with chemoresistance and loss of tumorigenicityStéphanie Struski, Martine Doco-Fenzy, Michael Koehler, et al.
Cancer Research|August 3, 2005
AF4p12, a human homologue to the furry gene of Drosophila, as a novel MLL fusion partnerSandrine Hayette, Pascale Cornillet-Lefebvre, Isabelle Tigaud, et al.
American Journal of Medical Genetics. Part A|January 18, 2006
Pure direct duplication (12)(q24.1-->q24.2) in a child with Marcus Gunn phenomenon and multiple congenital anomaliesMartine Doco-Fenzy, Pierre Mauran, Jean Marie Lebrun, et al.
Genes, Chromosomes & Cancer|September 12, 2018
Mutational and cytogenetic analyses of 188 CLL patients with trisomy 12: A retrospective study from the French Innovative Leukemia Organization (FILO) working groupDamien Roos-Weil, Florence Nguyen-Khac, Sylvie Chevret, et al.
Leukemia Research|May 2, 2009
Gain of the short arm of chromosome 2 (2p) is a frequent recurring chromosome aberration in untreated chronic lymphocytic leukemia (CLL) at advanced stagesElise Chapiro, Nathalie Leporrier, Isabelle Radford-Weiss, et al.
Pageof 3