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P. C. Freitas, Carvalho-Salles, A. B., Mendiburu, C. F., Ricci, Jr., O., and Fett-Conte, A. C., Clonal monosomy of chromosome 21 in a case of myelodysplastic syndrome, vol. 10. pp. 2718-2720, 2011.
Haase D (2008). Cytogenetic features in myelodysplastic syndromes. Ann. Hematol. 87: 515-526.    PMCid:2413090Haase D, Germing U, Schanz J, Pfeilstocker M, et al. (2007). New insights into the prognostic impact of the karyotype in MDS and correlation with subtypes: evidence from a core dataset of 2124 patients. Blood 110: 4385-4395. M and Hellstrom-Lindberg E (2009). Myelodysplastic syndromes: biology and treatment. J. Intern. Med. 265: 307-328. L and Nimer SD (2008). Myelodysplastic syndromes: diagnosis and staging. Cancer Control 15: 4-13.Mufti GJ, Bennett JM, Goasguen J, Bain BJ, et al. (2008). Diagnosis and classification of myelodysplastic syndrome: international working group on morphology of myelodysplastic syndrome (IWGM-MDS) consensus proposals for the definition and enumeration of myeloblasts and ring sideroblasts. Haematologica 93: 1712-1717. LG and Tommerup N (2009). An International System for Human Cytogenetic Nomenclature ISCN. ND-S Karger Publishers Inc., Basel.Wang H, Wang XQ, Xu XP and Lin GW (2010). Cytogenetic evolution correlates with poor prognosis in myelodysplastic syndrome. Cancer Genet. Cytogenet. 196: 159-166.