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Sangre
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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 disorders
F Solé, S Woessner, A Pérez-Losada, et al.
Cancer Genetics and Cytogenetics
|
July 15, 1994
Cytogenetic studies in five patients with Sézary syndrome
F Solé, S Woessner, T Vallespi, et al.
Haematologica
|
June 28, 2000
Application of cross-species color banding (RxFISH) in the study of T-prolymphocytic leukemia
B 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 lymphocytes
F 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.
Page
of 14
Search research articles
Search
Showing results (91-100 of 131) with videos related to
Sort By:
Page
of 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 disorders
F Solé, S Woessner, A Pérez-Losada, et al.
Cancer Genetics and Cytogenetics
|
July 15, 1994
Cytogenetic studies in five patients with Sézary syndrome
F Solé, S Woessner, T Vallespi, et al.
Haematologica
|
June 28, 2000
Application of cross-species color banding (RxFISH) in the study of T-prolymphocytic leukemia
B 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 lymphocytes
F 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.
Page
of 14