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Cancer Genetics and Cytogenetics
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June 20, 2002
Compilation of published comparative genomic hybridization studies
Stéphanie 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 FISH
Wei 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 leukemia
Yannick 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 tumorigenicity
Stéphanie 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 partner
Sandrine 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 anomalies
Martine 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 group
Damien 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 stages
Elise Chapiro, Nathalie Leporrier, Isabelle Radford-Weiss, et al.
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Search research articles
Search
Showing results (1-10 of 23) with videos related to
Sort By:
Page
of 3
Cancer Genetics and Cytogenetics
|
June 20, 2002
Compilation of published comparative genomic hybridization studies
Stéphanie 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 FISH
Wei 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 leukemia
Yannick 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 tumorigenicity
Stéphanie 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 partner
Sandrine 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 anomalies
Martine 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 group
Damien 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 stages
Elise Chapiro, Nathalie Leporrier, Isabelle Radford-Weiss, et al.
Page
of 3