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1. Doneda, L; Castorina, P; Tedeschi, A; Intropido, L; Morra, E; Montillo, M; Larizza, L
   Multicolor FISH in chronic lymphocytic leukemia. An interphase study of patients with early-onset disease
   CANCER GENETICS AND CYTOGENETICS
   
   L. Doneda et al., "Multicolor FISH in chronic lymphocytic leukemia. An interphase study of patients with early-onset disease", CANC GENET, 125(1), 2001, pp. 63-69
2. Castorina, P; Rodeschini, O; Nocera, G; Larizza, L
   Reproductive follow-up of carriers of familial reciprocal balanced translocations Involving chromosome 9 and comparison with predicted outcome
   GENETIC COUNSELING
   
   P. Castorina et al., "Reproductive follow-up of carriers of familial reciprocal balanced translocations Involving chromosome 9 and comparison with predicted outcome", GEN COUNSEL, 11(3), 2000, pp. 229-239
3. Beghini, A; Ripamonti, CB; Castorina, P; Pezzetti, L; Doneda, L; Cairoli, R; Morra, E; Larizza, L
   Trisomy 4 leading to duplication of a mutated KIT allele in acute myeloid leukemia with mast cell involvement
   CANCER GENETICS AND CYTOGENETICS
   
   A. Beghini et al., "Trisomy 4 leading to duplication of a mutated KIT allele in acute myeloid leukemia with mast cell involvement", CANC GENET, 119(1), 2000, pp. 26-31
4. Riva, P; Corrado, L; Natacci, F; Castorina, P; Wu, BL; Schneider, GH; Clementi, M; Tenconi, R; Korf, BR; Larizza, L
   NF1 microdeletion syndrome: Refined FISH characterization of sporadic and familial deletions with locus-specific probes
   AMERICAN JOURNAL OF HUMAN GENETICS
   
   P. Riva et al., "NF1 microdeletion syndrome: Refined FISH characterization of sporadic and familial deletions with locus-specific probes", AM J HU GEN, 66(1), 2000, pp. 100-109
5. CASTORINA P; MIOZZO M; MODIANO P; FURHMANCONTI AM; CROQUETTE MF; LARIZZA L
   HIGH-LEVEL TRISOMY-8 MOSAICISM IN PERIPHERAL-BLOOD LYMPHOCYTES FROM AROTHMUND-THOMSON-SYNDROME PATIENT
   European journal of human genetics
   
   P. Castorina et al., "HIGH-LEVEL TRISOMY-8 MOSAICISM IN PERIPHERAL-BLOOD LYMPHOCYTES FROM AROTHMUND-THOMSON-SYNDROME PATIENT", European journal of human genetics, 6, 1998, pp. 2062-2062
6. RIVA P; CORRADO L; CASTORINA P; COLAPIETRO P; LIDIA L
   REFINED CHARACTERIZATION OF THE DELETION IN AN NF1 PATIENT WITH A CONTIGUOUS GENE SYNDROME BY CONTIG YACS AND NOVEL 17Q11.2-Q12 STSS
   European journal of human genetics
   
   P. Riva et al., "REFINED CHARACTERIZATION OF THE DELETION IN AN NF1 PATIENT WITH A CONTIGUOUS GENE SYNDROME BY CONTIG YACS AND NOVEL 17Q11.2-Q12 STSS", European journal of human genetics, 6, 1998, pp. 4150-4150
7. BEGHINI A; CASTORINA P; CAIROLI R; RIPAMONTI C; MORRA E; LARIZZA L
   TRISOMY 4 AND C-KIT MUTATION IN A T(8-21) MYELOID-LEUKEMIA WITH MAST-CELL INVOLVEMENT
   Cytogenetics and cell genetics
   
   A. Beghini et al., "TRISOMY 4 AND C-KIT MUTATION IN A T(8-21) MYELOID-LEUKEMIA WITH MAST-CELL INVOLVEMENT", Cytogenetics and cell genetics, 81(2), 1998, pp. 160-160
8. MIOZZO M; CASTORINA P; RIVA P; DALPRA L; CONTI AMF; VOLPI L; HOE TS; KHOO A; WIEGANT J; ROSENBERG C; LARIZZA L
   CHROMOSOMAL INSTABILITY IN FIBROBLASTS AND MESENCHYMAL TUMORS FROM 2 SIBS WITH ROTHMUND-THOMSON-SYNDROME
   International journal of cancer
   
   M. Miozzo et al., "CHROMOSOMAL INSTABILITY IN FIBROBLASTS AND MESENCHYMAL TUMORS FROM 2 SIBS WITH ROTHMUND-THOMSON-SYNDROME", International journal of cancer, 77(4), 1998, pp. 504-510
9. CASTORINA P; MIOZZO M; RIVA P; CONTI AMF; WIEGANT J; ROSENBERG C; DALPRA L; VOLPI L; MAK JW; LARIZZA L
   HIGH CHROMOSOMAL INSTABILITY IN FIBROBLASTS AND MESENCHYMAL TUMORS FROM A SIBSHIP OF AN INBRED PEDIGREE WITH ROTHMUND-THOMSON SYNDROME (RTS)
   Cytogenetics and cell genetics
   
   P. Castorina et al., "HIGH CHROMOSOMAL INSTABILITY IN FIBROBLASTS AND MESENCHYMAL TUMORS FROM A SIBSHIP OF AN INBRED PEDIGREE WITH ROTHMUND-THOMSON SYNDROME (RTS)", Cytogenetics and cell genetics, 77(1-2), 1997, pp. 103-103
10. CASTORINA P; SELICORNI A; BEDESCHI F; DALPRA L; LARIZZA L
    GENOTYPE-PHENOTYPE CORRELATION IN 2 SETS OF MONOZYGOTIC TWINS WITH WILLIAMS-SYNDROME
    American journal of medical genetics
    
    P. Castorina et al., "GENOTYPE-PHENOTYPE CORRELATION IN 2 SETS OF MONOZYGOTIC TWINS WITH WILLIAMS-SYNDROME", American journal of medical genetics, 69(1), 1997, pp. 107-111
11. RIVA P; CORRADO L; CASTORINA P; MENEVERI R; LARIZZA L
    A CONTIG OF 18 MEGAYAC SPANNING THE 17Q11.2-12 REGION
    American journal of human genetics
    
    P. Riva et al., "A CONTIG OF 18 MEGAYAC SPANNING THE 17Q11.2-12 REGION", American journal of human genetics, 61(4), 1997, pp. 1408-1408
12. RIVA P; CASTORINA P; MANOUKIAN S; DALPRA L; DONEDA L; MARINI G; DENDUNNEN J; LARIZZA L
    CHARACTERIZATION OF A CYTOGENETIC 17Q11.2 DELETION IN AN NF1 PATIENT WITH A CONTIGUOUS GENE SYNDROME
    Human genetics
    
    P. Riva et al., "CHARACTERIZATION OF A CYTOGENETIC 17Q11.2 DELETION IN AN NF1 PATIENT WITH A CONTIGUOUS GENE SYNDROME", Human genetics, 98(6), 1996, pp. 646-650
13. LARIZZA L; RIVA P; CASTORINA P; DALPRA L; DONEDA L; MANOUKIAN S
    CYTOGENETIC AND MOLECULAR STUDIES ON NF1 PATIENTS WITH DYSMORPHISM AND MENTAL-RETARDATION
    American journal of human genetics
    
    L. Larizza et al., "CYTOGENETIC AND MOLECULAR STUDIES ON NF1 PATIENTS WITH DYSMORPHISM AND MENTAL-RETARDATION", American journal of human genetics, 57(4), 1995, pp. 521-521
14. CASTORINA P; DONNACHIE A; HARRIMAN PN
    NUCLEAR SHADOWING IN DEEP-INELASTIC SCATTERING AND DRELL-YAN PRODUCTION
    Zeitschrift fur Physik. C, Particles and fields
    
    P. Castorina et al., "NUCLEAR SHADOWING IN DEEP-INELASTIC SCATTERING AND DRELL-YAN PRODUCTION", Zeitschrift fur Physik. C, Particles and fields, 60(1), 1993, pp. 135-140