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Acta Haematologica
|
January 1, 1991
Acquired amegakaryocytic thrombocytopenic purpura associated with immunoglobulin deficiency
M Rovira, E Feliu, L Florensa, 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.
Sangre
|
January 1, 1985
[Practical use of the platelet peroxidase reaction at the ultrastructural level in the characterization of an apparently undifferentiated blast cell population]
R Lafuente, S Woessner, L Florensa, 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.
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.
The British Journal of Dermatology
|
September 27, 2005
Erythrokeratoderma variabilis-like ichthyosis in Chanarin-Dorfman syndrome
R M Pujol, M Gilaberte, A Toll, et al.
Medicina Clinica
|
October 20, 1984
[Acquired refractory anemia and neoplasms. Study of 11 cases]
J Sans-Sabrafen, J Buxó, S Woessner, et al.
Sangre
|
October 1, 1995
[Cytogenetic abnormalities in seven patients with the Sezary syndrome]
F Solé, S Woessner, T Vallespí, et al.
Cancer Genetics and Cytogenetics
|
November 1, 1992
Cytogenetic studies in 112 cases of untreated myelodysplastic syndromes
F Solé, F Prieto, L Badia, et al.
Page
of 14
Search research articles
Search
Showing results (101-110 of 136) with videos related to
Sort By:
Page
of 14
Acta Haematologica
|
January 1, 1991
Acquired amegakaryocytic thrombocytopenic purpura associated with immunoglobulin deficiency
M Rovira, E Feliu, L Florensa, 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.
Sangre
|
January 1, 1985
[Practical use of the platelet peroxidase reaction at the ultrastructural level in the characterization of an apparently undifferentiated blast cell population]
R Lafuente, S Woessner, L Florensa, 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.
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.
The British Journal of Dermatology
|
September 27, 2005
Erythrokeratoderma variabilis-like ichthyosis in Chanarin-Dorfman syndrome
R M Pujol, M Gilaberte, A Toll, et al.
Medicina Clinica
|
October 20, 1984
[Acquired refractory anemia and neoplasms. Study of 11 cases]
J Sans-Sabrafen, J Buxó, S Woessner, et al.
Sangre
|
October 1, 1995
[Cytogenetic abnormalities in seven patients with the Sezary syndrome]
F Solé, S Woessner, T Vallespí, et al.
Cancer Genetics and Cytogenetics
|
November 1, 1992
Cytogenetic studies in 112 cases of untreated myelodysplastic syndromes
F Solé, F Prieto, L Badia, et al.
Page
of 14