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Haematologica
|
June 15, 1999
Cytogenetic and in situ hybridization findings in 27 patients with atypical B-cell chronic lymphocytic leukaemia
B Espinet, F Solé, S Woessner, et al.
Leukemia Research
|
May 1, 1996
Trisomy 12 is a rare cytogenetic finding in typical chronic lymphocytic leukemia
S Woessner, F Solé, A Pérez-Losada, et al.
European Journal of Haematology
|
August 22, 2003
Congenital dyserthropoietic anaemia other than type I to III with a peculiar erythroblastic morphology
S Woessner, M Trujillo, L Florensa, et al.
Acta Haematologica
|
January 1, 1979
Chronic myelomonocytic leukemia associated with hereditary pyruvate kinase deficiency and multiple acquired erythrocyte abnormalities
J L Vives-Corrons, L Florensa, J Muncunill, et al.
Leukemia
|
August 2, 2001
Acute myeloid leukemia with 17p abnormality in untreated essential thrombocythemia
J A Hernández, L Florensa, F Solé, et al.
Sangre
|
April 1, 1989
[Type VII mucopolysaccharidosis (SLY disease)]
S Woessner, A Chavas, L Florensa, et al.
Blut
|
November 1, 1989
Hairy cell leukemia with ringed-shaped nuclei
S Woessner, R Lafuente, L Florensa, et al.
Haematologica
|
February 22, 2000
Absence of bcr/abl rearrangement in 41 patients with essential thrombocythemia
F Solé, L Florensa, B Espinet, et al.
Cancer Genetics and Cytogenetics
|
April 12, 2001
New t(11;12)(q12;q11) characterized by RxFISH in a patient with T-cell large granular lymphocyte leukemia
M Salido, F Solé, B Espinet, et al.
Sangre
|
April 1, 1993
[Selective chromosome painting using in situ hybridization]
A Pérez Losada, S Woessner, F Solé, et al.
Page
of 14
Search research articles
Search
Showing results (41-50 of 136) with videos related to
Sort By:
Page
of 14
Haematologica
|
June 15, 1999
Cytogenetic and in situ hybridization findings in 27 patients with atypical B-cell chronic lymphocytic leukaemia
B Espinet, F Solé, S Woessner, et al.
Leukemia Research
|
May 1, 1996
Trisomy 12 is a rare cytogenetic finding in typical chronic lymphocytic leukemia
S Woessner, F Solé, A Pérez-Losada, et al.
European Journal of Haematology
|
August 22, 2003
Congenital dyserthropoietic anaemia other than type I to III with a peculiar erythroblastic morphology
S Woessner, M Trujillo, L Florensa, et al.
Acta Haematologica
|
January 1, 1979
Chronic myelomonocytic leukemia associated with hereditary pyruvate kinase deficiency and multiple acquired erythrocyte abnormalities
J L Vives-Corrons, L Florensa, J Muncunill, et al.
Leukemia
|
August 2, 2001
Acute myeloid leukemia with 17p abnormality in untreated essential thrombocythemia
J A Hernández, L Florensa, F Solé, et al.
Sangre
|
April 1, 1989
[Type VII mucopolysaccharidosis (SLY disease)]
S Woessner, A Chavas, L Florensa, et al.
Blut
|
November 1, 1989
Hairy cell leukemia with ringed-shaped nuclei
S Woessner, R Lafuente, L Florensa, et al.
Haematologica
|
February 22, 2000
Absence of bcr/abl rearrangement in 41 patients with essential thrombocythemia
F Solé, L Florensa, B Espinet, et al.
Cancer Genetics and Cytogenetics
|
April 12, 2001
New t(11;12)(q12;q11) characterized by RxFISH in a patient with T-cell large granular lymphocyte leukemia
M Salido, F Solé, B Espinet, et al.
Sangre
|
April 1, 1993
[Selective chromosome painting using in situ hybridization]
A Pérez Losada, S Woessner, F Solé, et al.
Page
of 14