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F Mugneret

Showing results (21-30 of 66) with videos related to

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British Journal of Haematology|December 21, 2000
The 8p12 myeloproliferative disorder. t(8;19)(p12;q13.3): a novel translocation involving the FGFR1 geneF Mugneret, M Chaffanet, M Maynadié, et al.
Leukemia Research|November 22, 2000
Acute myeloid leukemia with hypergranular cytoplasm: a differential diagnosis of acute promyelocytic leukemiaF Girodon, P M Carli, B Favre, et al.
Hormone Research|January 1, 1992
The sole presence of the testis-determining region of the Y chromosome (SRY) in 46,XX patients is associated with phenotypic variabilityC Boucekkine, J E Toublanc, N Abbas, et al.
Annales De Genetique|April 24, 1999
Two cases of terminal deletion of chromosome 13: clinical features, conventional and molecular cytogenetic analysisI Luquet, B Favre, N Nadal, et al.
International Journal of Cancer|October 15, 1988
Establishment and characterization of three transplantable EBV-containing nasopharyngeal carcinomasP Busson, G Ganem, P Flores, et al.
Bone Marrow Transplantation|June 5, 1998
Prolonged remission and autologous recovery in two patients with chronic myelogenous leukemia after graft failure of allogeneic bone marrow transplantationL Fouillard, E Deconinck, P Tiberghien, et al.
Leukemia|November 9, 2000
MLL amplification in acute leukaemia: a United Kingdom Cancer Cytogenetics Group (UKCCG) studyG Cuthbert, K Thompson, S McCullough, et al.
Leukemia & Lymphoma|November 1, 1992
Bone marrow necrosis and human parvovirus associated infection preceding an Ph1+ acute lymphoblastic leukemiaT Petrella, F Bailly, F Mugneret, et al.
American Journal of Medical Genetics. Part A|May 17, 2007
Fortuitous FISH diagnosis of an interstitial microdeletion (5)(q31.1q31.2) in a girl suspected to present a cri-du-chat syndromeA L Mosca, P Callier, B Leheup, et al.
Leukemia|May 21, 1998
Ten novel 11q23 chromosomal partner sites. European 11q23 Workshop participantsC J Harrison, A Cuneo, R Clark, et al.
Pageof 7

Showing results (21-30 of 66) with videos related to

Sort By:
Pageof 7
British Journal of Haematology|December 21, 2000
The 8p12 myeloproliferative disorder. t(8;19)(p12;q13.3): a novel translocation involving the FGFR1 geneF Mugneret, M Chaffanet, M Maynadié, et al.
Leukemia Research|November 22, 2000
Acute myeloid leukemia with hypergranular cytoplasm: a differential diagnosis of acute promyelocytic leukemiaF Girodon, P M Carli, B Favre, et al.
Hormone Research|January 1, 1992
The sole presence of the testis-determining region of the Y chromosome (SRY) in 46,XX patients is associated with phenotypic variabilityC Boucekkine, J E Toublanc, N Abbas, et al.
Annales De Genetique|April 24, 1999
Two cases of terminal deletion of chromosome 13: clinical features, conventional and molecular cytogenetic analysisI Luquet, B Favre, N Nadal, et al.
International Journal of Cancer|October 15, 1988
Establishment and characterization of three transplantable EBV-containing nasopharyngeal carcinomasP Busson, G Ganem, P Flores, et al.
Bone Marrow Transplantation|June 5, 1998
Prolonged remission and autologous recovery in two patients with chronic myelogenous leukemia after graft failure of allogeneic bone marrow transplantationL Fouillard, E Deconinck, P Tiberghien, et al.
Leukemia|November 9, 2000
MLL amplification in acute leukaemia: a United Kingdom Cancer Cytogenetics Group (UKCCG) studyG Cuthbert, K Thompson, S McCullough, et al.
Leukemia & Lymphoma|November 1, 1992
Bone marrow necrosis and human parvovirus associated infection preceding an Ph1+ acute lymphoblastic leukemiaT Petrella, F Bailly, F Mugneret, et al.
American Journal of Medical Genetics. Part A|May 17, 2007
Fortuitous FISH diagnosis of an interstitial microdeletion (5)(q31.1q31.2) in a girl suspected to present a cri-du-chat syndromeA L Mosca, P Callier, B Leheup, et al.
Leukemia|May 21, 1998
Ten novel 11q23 chromosomal partner sites. European 11q23 Workshop participantsC J Harrison, A Cuneo, R Clark, et al.
Pageof 7