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Results: 1-25 | 26-26
Results: 1-25/26
FISH with locus-specific probes on stretched chromosomes: a useful tool for genome organization studies (vol 9, pg 167, 2001)
Authors: Bentivegna, A Venturin, M Gervasini, C Corrado, L Larizza, L Riva, P
Citation: A. Bentivegna et al., FISH with locus-specific probes on stretched chromosomes: a useful tool for genome organization studies (vol 9, pg 167, 2001), CHROMOS RES, 9(6), 2001, pp. 520-520
FISH with locus-specific probes on stretched chromosomes: A useful tool for genome organization studies
Authors: Bentivegna, A Venturin, M Gervasini, C Corrado, L Larizza, L Riva, P
Citation: A. Bentivegna et al., FISH with locus-specific probes on stretched chromosomes: A useful tool for genome organization studies, CHROMOS RES, 9(2), 2001, pp. 167-170
Identification of duplicated genes in 17q11.2 using FISH on stretched chromosomes and DNA fibers
Authors: Bentivegna, A Venturin, M Gervasini, C Corrado, L Larizza, L Riva, P
Citation: A. Bentivegna et al., Identification of duplicated genes in 17q11.2 using FISH on stretched chromosomes and DNA fibers, HUM GENET, 109(1), 2001, pp. 48-54
FISH characterization of t(8;12)(q12;p13) observed as the sole karyotypic anomaly in a myelodysplastic syndrome patient
Authors: Finelli, P Francchiolla, NS Giardino, D Gottardi, G Deliliers, DL Cortelezzi, A Larizza, L Deliliers, GL
Citation: P. Finelli et al., FISH characterization of t(8;12)(q12;p13) observed as the sole karyotypic anomaly in a myelodysplastic syndrome patient, CANC GENET, 130(1), 2001, pp. 75-78
Multicolor FISH in chronic lymphocytic leukemia. An interphase study of patients with early-onset disease
Authors: Doneda, L Castorina, P Tedeschi, A Intropido, L Morra, E Montillo, M Larizza, L
Citation: 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
Refilled FISH characterization of a de novo 1p22-p36.2 paracentric inversion and associated 1p21-22 deletion in a patient with signs of 1p36 microdeletion syndrome
Authors: Finelli, P Giardino, D Russo, S Gottardi, G Cogliati, F Grugni, G Natacci, F Larizza, L
Citation: P. Finelli et al., Refilled FISH characterization of a de novo 1p22-p36.2 paracentric inversion and associated 1p21-22 deletion in a patient with signs of 1p36 microdeletion syndrome, AM J MED G, 99(4), 2001, pp. 308-313
FISH characterization of a supernumerary r(1)(:: cen -> q22 :: q22 -> sq21::) chromosome associated with multiple anomalies and bilateral cataracts
Authors: Finelli, P Cavalli, P Giardino, D Gottardi, G Natacci, F Savasta, S Larizza, L
Citation: P. Finelli et al., FISH characterization of a supernumerary r(1)(:: cen -> q22 :: q22 -> sq21::) chromosome associated with multiple anomalies and bilateral cataracts, AM J MED G, 104(2), 2001, pp. 157-164
Germline mutation in the juxtamembrane domain of the kit gene in a family with gastrointestinal stromal tumors and urticaria pigmentosa
Authors: Beghini, A Tibiletti, M Roversi, G Chiaravalli, A Serio, G Capella, C Larizza, L
Citation: A. Beghini et al., Germline mutation in the juxtamembrane domain of the kit gene in a family with gastrointestinal stromal tumors and urticaria pigmentosa, CANCER, 92(3), 2001, pp. 657-662
Reproductive follow-up of carriers of familial reciprocal balanced translocations Involving chromosome 9 and comparison with predicted outcome
Authors: Castorina, P Rodeschini, O Nocera, G Larizza, L
Citation: 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
RNA hyperediting and alternative splicing of hematopoietic cell phosphatase (PTPN6) gene in acute myeloid leukemia
Authors: Beghini, A Ripamonti, CB Peterlongo, P Roversi, G Cairoli, R Morra, E Larizza, L
Citation: A. Beghini et al., RNA hyperediting and alternative splicing of hematopoietic cell phosphatase (PTPN6) gene in acute myeloid leukemia, HUM MOL GEN, 9(15), 2000, pp. 2297-2304
Maternal chromosome 7 hetero/isodisomy in Silver-Russell syndrome and PEG1biallelic expression
Authors: Russo, S Bedeschi, MF Cogliati, F Natacci, F Gianotti, A Parini, R Selicorni, A Larizza, L
Citation: S. Russo et al., Maternal chromosome 7 hetero/isodisomy in Silver-Russell syndrome and PEG1biallelic expression, CLIN DYSMOR, 9(3), 2000, pp. 157-162
Beneficial effect of fluoxetine in a case of sporadic hyperekplexia
Authors: Sechi, G Sotgiu, S Valenti, MP Pitzolu, MG Peterlongo, P Larizza, L Rosati, G
Citation: G. Sechi et al., Beneficial effect of fluoxetine in a case of sporadic hyperekplexia, CLIN NEUROP, 23(3), 2000, pp. 161-163
Delineation and physical separation of novel translocation breakpoints on chromosome 1p in two genetically closely associated childhood tumors
Authors: Steenman, MJC Zijlstra, N Kruitbosch, DL Wiesmeijer, C Larizza, L Voute, PA Westerveld, A Mannens, MMAM
Citation: Mjc. Steenman et al., Delineation and physical separation of novel translocation breakpoints on chromosome 1p in two genetically closely associated childhood tumors, CYTOG C GEN, 88(3-4), 2000, pp. 289-295
19p deletion in recurring leiomyosarcoma lesions from the same patient
Authors: Riva, P Dalpra, L Gualandri, V Volonte, M Miozzo, M Malgara, R Conti, AF Larizza, L
Citation: P. Riva et al., 19p deletion in recurring leiomyosarcoma lesions from the same patient, CANC GENET, 119(2), 2000, pp. 102-108
Trisomy 4 leading to duplication of a mutated KIT allele in acute myeloid leukemia with mast cell involvement
Authors: Beghini, A Ripamonti, CB Castorina, P Pezzetti, L Doneda, L Cairoli, R Morra, E Larizza, L
Citation: 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
Patient with large 17p11.2 deletion presenting with Smith-Magenis syndromeand Joubert syndrome phenotype
Authors: Natacci, F Corrado, L Pierri, M Rossetti, M Zuccarini, C Riva, P Miozzo, M Larizza, L
Citation: F. Natacci et al., Patient with large 17p11.2 deletion presenting with Smith-Magenis syndromeand Joubert syndrome phenotype, AM J MED G, 95(5), 2000, pp. 467-472
Mapping to distal Xq28 of nonspecific X-linked mental retardation MRX72: Linkage analysis and clinical findings in a three-generation Sardinian family
Authors: Russo, S Cogliati, F Cavalleri, F Cassitto, MG Giglioli, R Toniolo, D Casari, G Larizza, L
Citation: S. Russo et al., Mapping to distal Xq28 of nonspecific X-linked mental retardation MRX72: Linkage analysis and clinical findings in a three-generation Sardinian family, AM J MED G, 94(5), 2000, pp. 376-382
A tumor suppressor locus in familial and sporadic chordoma maps to 1p36
Authors: Miozzo, M Dalpra, L Riva, P Volonte, M Macciardi, F Pericotti, S Tibiletti, MG Cerati, M Rohde, K Larizza, L Conti, AMF
Citation: M. Miozzo et al., A tumor suppressor locus in familial and sporadic chordoma maps to 1p36, INT J CANC, 87(1), 2000, pp. 68-72
Non-random trisomies of chromosomes 5, 8 and 12 in the prolactinoma sub-type of pituitary adenomas: Conventional cytogenetics and interphase fish study
Authors: Finelli, P Giardino, D Rizzi, N Buiatiotis, S Virduci, T Franzin, A Losa, M Larizza, L
Citation: P. Finelli et al., Non-random trisomies of chromosomes 5, 8 and 12 in the prolactinoma sub-type of pituitary adenomas: Conventional cytogenetics and interphase fish study, INT J CANC, 86(3), 2000, pp. 344-350
C-kit mutations in core binding factor leukemias
Authors: Beghini, A Peterlongo, P Ripamonti, CB Larizza, L Cairoli, R Morra, E Mecucci, C
Citation: A. Beghini et al., C-kit mutations in core binding factor leukemias, BLOOD, 95(2), 2000, pp. 726-727
NF1 microdeletion syndrome: Refined FISH characterization of sporadic and familial deletions with locus-specific probes
Authors: Riva, P Corrado, L Natacci, F Castorina, P Wu, BL Schneider, GH Clementi, M Tenconi, R Korf, BR Larizza, L
Citation: 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
Distribution and high frequency of novel alleles at NF1 polymorphic markers in the Italian population
Authors: Natacci, F Colapietro, P Riva, P Corrado, L Rossi, LN Maninetti, MM Casciati, MC Zambrino, CA Lanzi, G Larizza, L
Citation: F. Natacci et al., Distribution and high frequency of novel alleles at NF1 polymorphic markers in the Italian population, MOL CELL PR, 13(6), 1999, pp. 415-420
FISH characterization of two supernumerary r(1) associated with distinct clinical phenotypes
Authors: Giardino, D Bettio, D Gottardi, G Rizzi, N Pierluigi, M Perfumo, C Cali, A Bricarelli, FD Larizza, L
Citation: D. Giardino et al., FISH characterization of two supernumerary r(1) associated with distinct clinical phenotypes, AM J MED G, 84(4), 1999, pp. 377-380
New case of the Richieri-Costa/Guion-Almeida syndrome
Authors: Natacci, F Pierri, M Rossetti, M Sala, M Larizza, L
Citation: F. Natacci et al., New case of the Richieri-Costa/Guion-Almeida syndrome, AM J MED G, 83(5), 1999, pp. 419-421
First cytogenetic study of a recurrent familial chordoma of the clivus
Authors: Dalpra, L Malgara, R Miozzo, M Riva, P Volonte, M Larizza, L Conti, AMF
Citation: L. Dalpra et al., First cytogenetic study of a recurrent familial chordoma of the clivus, INT J CANC, 81(1), 1999, pp. 24-30
Risultati: 1-25 | 26-26