A case of chronic myelocytic leukemia with five Philadelphia chromosomesCASALONE, R; MASERATI, E.Cancer genetics and cytogenetics. 1988, Vol 34, Num 2, pp 257-259, issn 0165-4608Article

Stimulation of DNA synthesis by endothelin-1 in primary cultures of human dental pulpCASASCO, A; MASERATI, E; POLAK, J. M et al.Archives of oral biology. 1994, Vol 39, Num 3, pp 245-249, issn 0003-9969Article

Graft-versus-leukemia effects after allogeneic bone marrow transplantation are active also in the presence of clones with chromosomal anomalies in addition to the Ph chromosomeMASERATI, E; CASALI, M; FOGU, G et al.Cancer genetics and cytogenetics. 1992, Vol 61, Num 2, pp 152-157, issn 0165-4608Article

Ring chromosome 9 with a 9p22.3-p24.3 duplicationSEGHEZZI, L; MARASCHIO, P; BOZZOLA, M et al.European journal of pediatrics. 1999, Vol 158, Num 10, pp 791-793, issn 0340-6199Article

Definition of an acquired 11q deletion in a tumorigenic human monocytic cell lineMASERATI, E; ROMITTI, L; CARROZZA, M. L et al.Human genetics. 1990, Vol 84, Num 4, pp 381-381, issn 0340-6717, 1 p.Article

Transferrin and structural anomalies of chromosome 3 in the blastic phase of chronic myelocytic leukemiaMASERATI, E; CAMPAGNOLI, E; TRUGLIO, F et al.Hereditas (Landskrona). 1989, Vol 111, Num 3, pp 305-308, issn 0018-0661Article

The isochromosome i(7)(q10) carrying c.258+2t>c mutation of the SBDS gene does not promote development of myeloid malignancies in patients with Shwachman syndromeMINELLI, A; MASERATI, E; CIPOLLI, M et al.Leukemia. 2009, Vol 23, Num 4, pp 708-711, issn 0887-6924, 4 p.Article

Centralized cytogenetic analysis of pediatric acute leukemia : Results of an Italian collaborative experienceSAINATI, L; LESZL, A; STELLA, M et al.Haematologica (Roma). 1997, Vol 82, Num 6, pp 654-659, issn 0390-6078Article

Busulfan, cyclophosphamide and melphalan as conditioning regimen for bone marrow transplantation in children with myelodysplastic syndromesLOCATELLI, F; PESSION, A; BONETTI, F et al.Leukemia. 1994, Vol 8, Num 5, pp 844-849, issn 0887-6924Article

Clinical, cytogenetic and immunological aspects in 4 cases resembling ataxia telangiectasiaLANZI, G; BALOTTIN, U; FRANCIOTTA, D et al.European neurology. 1992, Vol 32, Num 3, pp 121-125, issn 0014-3022Article

Cytogenetics in autologous bone marrow transplantationMASERATI, E; CAMPAGNOLI, E; TRUGLIO, F et al.Cancer genetics and cytogenetics. 1990, Vol 45, Num 1, pp 137-138, issn 0165-4608, 2 p.Article

Myelodysplastic syndromes : the pediatric point of viewLOCATELLI, F; ZECCA, M; PESSION, A et al.Haematologica (Roma). 1995, Vol 80, Num 3, pp 268-279, issn 0390-6078Article

Roberts syndrome : phenotypic variation, cytogenetic definition and heterozygote detectionMASERATI, E; PASQUALI, F; ZUFFARDI, O et al.Annales de génétique (Paris). 1991, Vol 34, Num 3-4, pp 239-246, issn 0003-3995Article

A highly conserved sequence on the short arm of chromosome 7 detects multiple polymorphismsBARDONI, B; GUIOLI, S; MASERATI, E et al.Human genetics. 1988, Vol 81, Num 1, pp 23-25, issn 0340-6717Article

Ataxia-without-telangiectasia in two sisters with rearrangements of chromosomes 7 and 14MASERATI, E; OTTOLINI, A; VEGGIOTTI, P et al.Clinical genetics. 1988, Vol 34, Num 5, pp 283-287, issn 0009-9163Article

A 45,X male with a Yp/18 translocationMASERATI, E; WAIBEL, F; WOLF, U et al.Human genetics. 1986, Vol 74, Num 2, pp 126-132, issn 0340-6717Article