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Results: 1-10 |
Results: 10
HIGH-LEVEL TRISOMY-8 MOSAICISM IN PERIPHERAL-BLOOD LYMPHOCYTES FROM AROTHMUND-THOMSON-SYNDROME PATIENT
Authors: CASTORINA P MIOZZO M MODIANO P FURHMANCONTI AM CROQUETTE MF LARIZZA L
Citation: 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
REFINED CHARACTERIZATION OF THE DELETION IN AN NF1 PATIENT WITH A CONTIGUOUS GENE SYNDROME BY CONTIG YACS AND NOVEL 17Q11.2-Q12 STSS
Authors: RIVA P CORRADO L CASTORINA P COLAPIETRO P LIDIA L
Citation: 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
TRISOMY 4 AND C-KIT MUTATION IN A T(8-21) MYELOID-LEUKEMIA WITH MAST-CELL INVOLVEMENT
Authors: BEGHINI A CASTORINA P CAIROLI R RIPAMONTI C MORRA E LARIZZA L
Citation: 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
CHROMOSOMAL INSTABILITY IN FIBROBLASTS AND MESENCHYMAL TUMORS FROM 2 SIBS WITH ROTHMUND-THOMSON-SYNDROME
Authors: MIOZZO M CASTORINA P RIVA P DALPRA L CONTI AMF VOLPI L HOE TS KHOO A WIEGANT J ROSENBERG C LARIZZA L
Citation: 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
HIGH CHROMOSOMAL INSTABILITY IN FIBROBLASTS AND MESENCHYMAL TUMORS FROM A SIBSHIP OF AN INBRED PEDIGREE WITH ROTHMUND-THOMSON SYNDROME (RTS)
Authors: CASTORINA P MIOZZO M RIVA P CONTI AMF WIEGANT J ROSENBERG C DALPRA L VOLPI L MAK JW LARIZZA L
Citation: 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
GENOTYPE-PHENOTYPE CORRELATION IN 2 SETS OF MONOZYGOTIC TWINS WITH WILLIAMS-SYNDROME
Authors: CASTORINA P SELICORNI A BEDESCHI F DALPRA L LARIZZA L
Citation: 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
A CONTIG OF 18 MEGAYAC SPANNING THE 17Q11.2-12 REGION
Authors: RIVA P CORRADO L CASTORINA P MENEVERI R LARIZZA L
Citation: 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
CHARACTERIZATION OF A CYTOGENETIC 17Q11.2 DELETION IN AN NF1 PATIENT WITH A CONTIGUOUS GENE SYNDROME
Authors: RIVA P CASTORINA P MANOUKIAN S DALPRA L DONEDA L MARINI G DENDUNNEN J LARIZZA L
Citation: 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
CYTOGENETIC AND MOLECULAR STUDIES ON NF1 PATIENTS WITH DYSMORPHISM AND MENTAL-RETARDATION
Authors: LARIZZA L RIVA P CASTORINA P DALPRA L DONEDA L MANOUKIAN S
Citation: 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
NUCLEAR SHADOWING IN DEEP-INELASTIC SCATTERING AND DRELL-YAN PRODUCTION
Authors: CASTORINA P DONNACHIE A HARRIMAN PN
Citation: 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
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