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S Woessner

Showing results (161-170 of 189) with videos related to

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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.
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 lymphocytesF Solé, B Espinet, M Salido, et al.
Acta Haematologica|January 1, 1974
Congenital dyserythropoietic anaemia type II. Clinical and ultrastructural studyC 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 myelofibrosisF Solé, J M de Pablos, S Woessner, et al.
Pageof 19

Showing results (161-170 of 189) with videos related to

Sort By:
Pageof 19
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.
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 lymphocytesF Solé, B Espinet, M Salido, et al.
Acta Haematologica|January 1, 1974
Congenital dyserythropoietic anaemia type II. Clinical and ultrastructural studyC 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 myelofibrosisF Solé, J M de Pablos, S Woessner, et al.
Pageof 19