Sfoglia per Autore
Involvement of unstable chromosomal regions containing C-heterochromatin and fragile sites in the integration of amplified dhfr domains
1989 P. Riva, C. De Giuli Morghen, L. Larizza
Monosomia del cromosoma 22 e perdita allelica al locus polimorfico c-sis nel meningioma.
1990 P. Riva, L. Doneda, P. Guerra, L. Larizza
Expression of c-sis and c-fos genes in human meningiomas and neurinomas
1992 P. Riva, L. Larizza
On the paternal origin of the chromosomes in a 49,XXXXX fetus.
1994 L. Volpi, P. Riva, L. Dalprà, M.G. Tibiletti, P. Vergani, L. Larizza
Satellite DNA sequences flank amplified DHFR domains in marker chromosomes of mouse fibrosarcoma cells
1994 P. Riva, S. Orlando, T. Labella, L. Larizza
A 12-bp deletion (7818del12) in the c-kit protooncogene in a large Italian kindred with piebaldism
1995 P. Riva, N. Milani, P. Gandolfi, L. Larizza
Isochromosome 15q of maternal origin in a Prader-Willi patient with pituitary adenoma
1996 D. Bettio, D. Giardino, N. Rizzi, P. Riva, L. Volpi, E. Barantani, A. Tagliaferri, L. Larizza
A novel potentially diagnostic polymorphism (4894 A/C) in exon 10 of the human c-kit proto-oncogene
1996 P. Riva, L. Larizza
FISH characterization of the Xq21 breakpoint in a translocation carrier with premature ovarian failure
1996 P. Riva, I. Magnani, A. M. Fuhrman Conti, D. Gelli, C. Sala, D. Toniolo, L. Larizza
Characterization of a cytogenetic 17q11.2 deletion in an NF1 patient with a contiguous gene syndrome
1996 P. Riva, P. Castorina, S. Manoukian, L. Dalprà, L. Doneda, G. Marini, J. den Dunnen, L. Larizza
Eleven X chromosome breakpoints associated with premature ovarian failure (POF) map to a 15-Mb YAC contig spanning Xq21
1997 C. Sala, G. Arrigo, G. Torri, F. Martinazzi, P. Riva, L. Larizza, C. Philippe, P. Jonveaux, F. Sloan, T. Labella, D. Toniolo
Un metodo rapido e semplice per generare sonde locus-specifiche per l’analisi mediante FISH
1998 P. Riva, L. Corrado
Chromosomal instability in fibroblasts and mesenchymal tumors from 2 sibs with Rothmund-Thomson syndrome
1998 M. Miozzo, P. Castorina, P. Riva, L. Dalprà, A. M. Fuhrman Conti, L. Volpi, T. S. Hoe, A. Khoo, J. Wiegant, C. Rosenberg, L. Larizza
First cytogenetic study of a recurrent familial chordoma of the clivus
1999 L. Dalprà, R. Malgara, M. Miozzo, P. Riva, M. Volontè, L. Larizza, A. M. Fuhrman Conti
Mapping of human WHN gene in a 17q11.2 YAC contig and identification of an intragenic STR
1999 L. Corrado, P. Colapietro, L. Larizza, P. Riva
Distribution and high frequency of novel alleles at NF1 polymorphic markers in the Italian population
1999 F. Natacci, P. Colapietro, P. Riva, L. Corrado, L.N. Rossi, M.M. Maninetti, M.C. Casciati, C.A. Zambrino, G. Lanzi, L. Larizza
Mapping of genes and EST to 17q11.2 to a YAC contig centered on the NF1 gene
2000 L. Corrado, P. Riva, M. Venturin, A. Bentivegna, C. Gervasini, L. Larizza
NF1 microdeletion syndrome: refined FISH characterization of sporadic and familial deletions with locus-specific probes
2000 P. Riva, L. Corrado, F. Natacci, P. Castorina, B. L. Wu, G. H. Schneider, M. Clementi, R. Tenconi, B. R. Korf, L. Larizza
19p deletion in recurring leiomyosarcoma lesions from the same patient
2000 P. Riva, L. Dalprá, V. Gualandri, M. Volontè, M. Miozzo, R. Malgara, A. F. Conti, L. Larizza
A tumor suppressor locus in familial and sporadic chordoma maps to 1p36
2000 M. Miozzo, L. Dalprà, P. Riva, M. Volontè, F. Macciardi, S. Pericotti, M. G. Tibiletti, M. Cerati, K. Rohde, L. Larizza, A. M. Fuhrman Conti
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