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F Solé

Showing results (81-90 of 131) with videos related to

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Cancer Genetics and Cytogenetics|November 7, 2000
Cytogenetic and fluorescence in situ hybridization studies in four cases of plasma cell leukemiaE Lloveras, F Solé, B Espinet, et al.
Cancer Genetics and Cytogenetics|February 1, 1996
Cytogenetic abnormalities in 13 patients with multiple myelomaF Solé, S Woessner, P Acín, et al.
Cytogenetic and Genome Research|September 29, 2007
Duplication dup(1)(q41q44) defined by fluorescence in situ hybridization: delineation of the 'trisomy 1q42-->qter syndrome'M C Coccé, O Villa, M G Obregon, et al.
Actas Urologicas Espanolas|September 1, 1983
[Value of computerized axial tomography in the diagnosis of the invasiveness and follow-up of patients with testicular cancer]J R Germa Liuch, M Gallen, C Alexander Dupleich, et al.
European Journal of Haematology|June 23, 2000
Isochromosome +i(3)(q10) in a new case of persistent polyclonal B-cell lymphocytosis (PPBL)B Espinet, L Florensa, F Solé, et al.
Cancer Genetics and Cytogenetics|June 1, 1992
Cytogenetic studies in acute nonlymphocytic leukemiaF Solé, M R Caballín, M D Coll, et al.
Cancer Genetics and Cytogenetics|October 15, 1994
Refractory anemia with excess of blasts and isochromosome 12p in a patient with primary mediastinal germ-cell tumorF Solé, F Bosch, S Woessner, et al.
Cancer Genetics and Cytogenetics|April 13, 1999
Cytogenetic findings in five patients with hairy cell leukemiaF Solé, S Woessner, L Florensa, et al.
Cancer Genetics and Cytogenetics|February 1, 1990
Cytogenetic study of a patient with the Sézary syndromeF Solé, N Tarrida, M D Coll, et al.
Prenatal Diagnosis|December 18, 2001
A female infant with a 46,XX/48,XY, +8, +10 karyotype in prenatal diagnosis: a 'vanishing twin' phenomenon?E Lloveras, J M Lecumberri, C Pérez, et al.
Pageof 14

Showing results (81-90 of 131) with videos related to

Sort By:
Pageof 14
Cancer Genetics and Cytogenetics|November 7, 2000
Cytogenetic and fluorescence in situ hybridization studies in four cases of plasma cell leukemiaE Lloveras, F Solé, B Espinet, et al.
Cancer Genetics and Cytogenetics|February 1, 1996
Cytogenetic abnormalities in 13 patients with multiple myelomaF Solé, S Woessner, P Acín, et al.
Cytogenetic and Genome Research|September 29, 2007
Duplication dup(1)(q41q44) defined by fluorescence in situ hybridization: delineation of the 'trisomy 1q42-->qter syndrome'M C Coccé, O Villa, M G Obregon, et al.
Actas Urologicas Espanolas|September 1, 1983
[Value of computerized axial tomography in the diagnosis of the invasiveness and follow-up of patients with testicular cancer]J R Germa Liuch, M Gallen, C Alexander Dupleich, et al.
European Journal of Haematology|June 23, 2000
Isochromosome +i(3)(q10) in a new case of persistent polyclonal B-cell lymphocytosis (PPBL)B Espinet, L Florensa, F Solé, et al.
Cancer Genetics and Cytogenetics|June 1, 1992
Cytogenetic studies in acute nonlymphocytic leukemiaF Solé, M R Caballín, M D Coll, et al.
Cancer Genetics and Cytogenetics|October 15, 1994
Refractory anemia with excess of blasts and isochromosome 12p in a patient with primary mediastinal germ-cell tumorF Solé, F Bosch, S Woessner, et al.
Cancer Genetics and Cytogenetics|April 13, 1999
Cytogenetic findings in five patients with hairy cell leukemiaF Solé, S Woessner, L Florensa, et al.
Cancer Genetics and Cytogenetics|February 1, 1990
Cytogenetic study of a patient with the Sézary syndromeF Solé, N Tarrida, M D Coll, et al.
Prenatal Diagnosis|December 18, 2001
A female infant with a 46,XX/48,XY, +8, +10 karyotype in prenatal diagnosis: a 'vanishing twin' phenomenon?E Lloveras, J M Lecumberri, C Pérez, et al.
Pageof 14