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La ricerca find articoli where authors phrase all words ' CASTORINA P' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 14 riferimenti
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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
    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
    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
    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
    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
    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
    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
    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
    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
    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
    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
    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
    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
    14. CASTORINA P; DONNACHIE A; HARRIMAN PN
      NUCLEAR SHADOWING IN DEEP-INELASTIC SCATTERING AND DRELL-YAN PRODUCTION

      Zeitschrift fur Physik. C, Particles and fields


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 18/01/21 alle ore 03:04:21