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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|August 14, 2009
MYC gene numerical aberrations in actinic keratosis and cutaneous squamous cell carcinomaA Toll, R Salgado, M Yébenes, et al.Cancer Genetics and Cytogenetics|November 1, 1992
Cytogenetic studies in 112 cases of untreated myelodysplastic syndromesF Solé, F Prieto, L Badia, et al.Blood|August 1, 1991
Trisomy 12 in chronic lymphocytic leukemia: an interphase cytogenetic studyA P Losada, M Wessman, M Tiainen, et al.American Journal of Medical Genetics. Part A|January 22, 2004
Two cases of tetrasomy 9p syndrome with tissue limited mosaicismElisabet Lloveras, C Pérez, F Solé, et al.Leukemia|May 16, 2008
Gene expression profiling distinguishes JAK2V617F-negative from JAK2V617F-positive patients in essential thrombocythemiaE Puigdecanet, B Espinet, J J Lozano, et al.Leukemia|February 20, 1999
Major vascular complications in essential thrombocythemia: a study of the predictive factors in a series of 148 patientsC Besses, F Cervantes, A Pereira, et al.British Journal of Haematology|February 26, 2000
Incidence, characterization and prognostic significance of chromosomal abnormalities in 640 patients with primary myelodysplastic syndromes. Grupo Cooperativo Español de Citogenética HematológicaF Solé, B Espinet, G F Sanz, et al.The British Journal of Dermatology|July 29, 2010
Multiple genetic copy number alterations in oral squamous cell carcinoma: study of MYC, TP53, CCDN1, EGFR and ERBB2 status in primary and metastatic tumoursG Martín-Ezquerra, R Salgado, A Toll, et al.Pageof 13