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F Solé

Showing results (91-100 of 131) with videos related to

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Sangre|December 30, 1998
[Interstitial 9q deletion: a primary change in acute non-lymphoblastic leukemia?]E Lloveras, F Solé, L Florensa, et al.
Cancer Genetics and Cytogenetics|February 1, 1997
Cytogenetic studies in seventy-six cases of B-chronic lymphoproliferative disordersF Solé, S Woessner, A Pérez-Losada, et al.
Cancer Genetics and Cytogenetics|July 15, 1994
Cytogenetic studies in five patients with Sézary syndromeF Solé, S Woessner, T Vallespi, et al.
Haematologica|June 28, 2000
Application of cross-species color banding (RxFISH) in the study of T-prolymphocytic leukemiaB Espinet, F Solé, M Salido, et al.
Actas Urologicas Espanolas|January 1, 1977
[Diagnostic pattern in nonpalpable testicles]J F Jiménez, A Soler-Roselló, M Gómez-Agudo, et al.
British Journal of Haematology|August 10, 2000
Translocation t(6;14)(p12;q32): a novel cytogenetic abnormality in splenic lymphoma with villous lymphocytesF Solé, B Espinet, M Salido, et al.
Actas Dermo-Sifiliograficas|March 25, 2008
[Analysis of cytogenetic abnormalities in squamous cell carcinoma by array comparative genomic hybridization]R Salgado, A Toll, B Espinet, et al.
Medicina Clinica|April 16, 1998
[Cytogenetic study of 93 myelodysplastic syndromes]F Solé, S Woessner, L Florensa, et al.
Leukemia Research|August 1, 1993
Isochromosome 17q as a sole anomaly: a distinct myelodysplastic syndrome entity?F Solé, M Torrabadella, I Granada, et al.
Sangre|October 1, 1995
[Cytogenetic abnormalities in seven patients with the Sezary syndrome]F Solé, S Woessner, T Vallespí, et al.
Pageof 14

Showing results (91-100 of 131) with videos related to

Sort By:
Pageof 14
Sangre|December 30, 1998
[Interstitial 9q deletion: a primary change in acute non-lymphoblastic leukemia?]E Lloveras, F Solé, L Florensa, et al.
Cancer Genetics and Cytogenetics|February 1, 1997
Cytogenetic studies in seventy-six cases of B-chronic lymphoproliferative disordersF Solé, S Woessner, A Pérez-Losada, et al.
Cancer Genetics and Cytogenetics|July 15, 1994
Cytogenetic studies in five patients with Sézary syndromeF Solé, S Woessner, T Vallespi, et al.
Haematologica|June 28, 2000
Application of cross-species color banding (RxFISH) in the study of T-prolymphocytic leukemiaB Espinet, F Solé, M Salido, et al.
Actas Urologicas Espanolas|January 1, 1977
[Diagnostic pattern in nonpalpable testicles]J F Jiménez, A Soler-Roselló, M Gómez-Agudo, et al.
British Journal of Haematology|August 10, 2000
Translocation t(6;14)(p12;q32): a novel cytogenetic abnormality in splenic lymphoma with villous lymphocytesF Solé, B Espinet, M Salido, et al.
Actas Dermo-Sifiliograficas|March 25, 2008
[Analysis of cytogenetic abnormalities in squamous cell carcinoma by array comparative genomic hybridization]R Salgado, A Toll, B Espinet, et al.
Medicina Clinica|April 16, 1998
[Cytogenetic study of 93 myelodysplastic syndromes]F Solé, S Woessner, L Florensa, et al.
Leukemia Research|August 1, 1993
Isochromosome 17q as a sole anomaly: a distinct myelodysplastic syndrome entity?F Solé, M Torrabadella, I Granada, et al.
Sangre|October 1, 1995
[Cytogenetic abnormalities in seven patients with the Sezary syndrome]F Solé, S Woessner, T Vallespí, et al.
Pageof 14