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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.
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
|
January 1, 1980
[Ultrastructural study of intra-erythrocyte inclusions in some haemolytic syndrome (author's transl)]
E Feliu, C Rozman, J L Aguilar, 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.
Acta Haematologica
|
January 1, 1974
Congenital dyserythropoietic anaemia type II. Clinical and ultrastructural study
C Rozman, S Woessner, M Ribas-Mundó, 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
|
April 1, 1997
Coexistence of tetrasomy 8 and trisomy 8 in a case with myeloid metaplasia with myelofibrosis
F Solé, J M de Pablos, S Woessner, et al.
Page
of 19
Search research articles
Search
Showing results (161-170 of 189) with videos related to
Sort By:
Page
of 19
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.
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
|
January 1, 1980
[Ultrastructural study of intra-erythrocyte inclusions in some haemolytic syndrome (author's transl)]
E Feliu, C Rozman, J L Aguilar, 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.
Acta Haematologica
|
January 1, 1974
Congenital dyserythropoietic anaemia type II. Clinical and ultrastructural study
C Rozman, S Woessner, M Ribas-Mundó, 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
|
April 1, 1997
Coexistence of tetrasomy 8 and trisomy 8 in a case with myeloid metaplasia with myelofibrosis
F Solé, J M de Pablos, S Woessner, et al.
Page
of 19