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Fluorescence in situ hybridization improves the detection of 5q31 deletion in myelodysplastic syndromes without cytogenetic evidence of 5q-.
Mallo M, Arenillas L, Espinet B, Salido M, Hernández JM, Lumbreras E, del Rey M, Arranz E, Ramiro S, Font P, González O, Renedo M, Cervera J, Such E, Sanz GF, Luño E, Sanzo C, González M, Calasanz MJ, Mayans J, García-Ballesteros C, Amigo V, Collado R, Oliver I, Carbonell F, Bureo E, Insunza A, Yañez L, Muruzabal MJ, Gómez-Beltrán E, Andreu R, León P, Gómez V, Sanz A, Casasola N, Moreno E, Alegre A, Martín ML, Pedro C, Serrano S, Florensa L, Solé F. Mallo M, et al. Among authors: sole f. Haematologica. 2008 Jul;93(7):1001-8. doi: 10.3324/haematol.13012. Haematologica. 2008. PMID: 18591625 Free article.
Trisomy 13 in a patient with a myelodysplastic syndrome.
Solé F, Woessner S, Acin P, Páez A, Pérez-Losada A, Florensa L, Sans-Sabrafen J. Solé F, et al. Cancer Genet Cytogenet. 1995 Jun;81(2):185. doi: 10.1016/0165-4608(94)00098-v. Cancer Genet Cytogenet. 1995. PMID: 7621420 No abstract available.
Burkitt's type translocation in multiple myeloma.
Solé F, Woessner S, Acín P, Pérez-Losada A, Florensa L, Besses C, Sans-Sabrafen J. Solé F, et al. Leuk Res. 1994 Sep;18(9):671-3. doi: 10.1016/0145-2126(94)90066-3. Leuk Res. 1994. PMID: 7934142
Cytogenetic studies in five patients with Sézary syndrome.
Solé F, Woessner S, Vallespi T, Pérez Losada A, Florensa L, Irriguible D, Vila J, Sans-Sabrafen J. Solé F, et al. Cancer Genet Cytogenet. 1994 Jul 15;75(2):130-2. doi: 10.1016/0165-4608(94)90164-3. Cancer Genet Cytogenet. 1994. PMID: 8055476
396 results