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Cancer Genetics and Cytogenetics|April 1, 1989
Malformation syndrome with t(2;22) in a cancer family with chromosome instabilityI Magnani, L Larizza, L Doneda, et al.Journal of Neurology|June 1, 1986
Cytogenetic analysis and muscle differentiation in a girl with severe muscular dystrophyG Meola, E Scarpini, M Velicogna, et al.American Journal of Medical Genetics|January 10, 1997
FISH characterization of small supernumerary marker chromosomes in two Prader-Willi patientsD Bettio, N Rizzi, D Giardino, et al.European Journal of Cancer & Clinical Oncology|September 1, 1982
Expression of transformation markers and suppression of tumorigenicity in human cell hybridsL Larizza, M L Tenchini, A Mottura, et al.European Journal of Human Genetics : EJHG|February 13, 2002
Cryptic subtelomeric translocation t(2;16)(q37;q24) segregating in a family with unexplained stillbirths and a dysmorphic, slightly retarded childD Giardino, P Finelli, G Gottardi, et al.Cancer Genetics and Cytogenetics|April 12, 2001
Multicolor FISH in chronic lymphocytic leukemia. An interphase study of patients with early-onset diseaseL Doneda, P Castorina, A Tedeschi, et al.Annales De Genetique|June 1, 1975
A family with three sibs carrying trisomy 21F Nuzzo, M Stefanini, G Simoni, et al.American Journal of Medical Genetics|December 18, 2001
FISH characterization of a supernumerary r(1)(::cen-->q22::q22-->sq21::) chromosome associated with multiple anomalies and bilateral cataractsP Finelli, P Cavalli, D Giardino, et al.Cancer Letters|January 13, 2015
Suggestive evidence on the involvement of polypyrimidine-tract binding protein in regulating alternative splicing of MAP/microtubule affinity-regulating kinase 4 in gliomaL Fontana, D Rovina, C Novielli, et al.Human Genetics|July 18, 1979
Chromosome lesions in amniotic fluid cell culturesG Simoni, L Larizza, N Sacchi, et al.Pageof 11