C. Mecucci

发表

TEL gene is involved in myelodysplastic syndromes with either the typical t(5;12)(q33;p13) translocation or its variant t(10;12)(q24;p13).

P. Marynen, A. Aventín, C. Mecucci, 1995, Blood.

FIP1L1-PDGFRA in chronic eosinophilic leukemia and BCR-ABL1 in chronic myeloid leukemia affect different leukemic cells

P. Marynen, C. Mecucci, M. Martelli, 2007, Leukemia.

Role of BCL2L10 methylation and TET2 mutations in higher risk myelodysplastic syndromes treated with 5-Azacytidine

M. Vignetti, M. Voso, S. Hohaus, 2011, Leukemia.

Simultaneous detection of NPM1 and FLT3-ITD mutations by capillary electrophoresis in acute myeloid leukemia

B. Falini, F. Lo‐Coco, C. Mecucci, 2005, Leukemia.

Characterization of a recurrent translocation t(2;3)(p15–22;q26) occurring in acute myeloid leukaemia

M. Mancini, M. Rocchi, G. Specchia, 2006, Leukemia.

CALM/AF10-positive leukemias show upregulation of genes involved in chromatin assembly and DNA repair processes and of genes adjacent to the breakpoint at 10p12

C. Lottaz, C. Buske, S. Bohlander, 2012, Leukemia.

CIZ gene rearrangements in acute leukemia: report of a diagnostic FISH assay and clinical features of nine patients

P. Marynen, A. Hagemeijer, R. Foà, 2005, Leukemia.

The prognostic value of cytogenetics is reinforced by the kind of induction/consolidation therapy in influencing the outcome of acute myeloid leukemia – analysis of 848 patients

M. Gobbi, R. Fanin, F. Mandelli, 2001, Leukemia.

A novel germline mutation in CDK4 codon 24 associated to familial melanoma

I. Bottillo, A. Paiardini, S. Bargiacchi, 2018, Clinical genetics.

3q aberration and monosomy 7 in ANLL presenting with high platelet count and diabetes insipidus.

D. Falzetti, C. Mecucci, A. Tabilio, 1994, Haematologica.