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Mostrati risultati da 1 a 20 di 134
Titolo Data di pubblicazione Autori Tipo File Abstract
Involvement of unstable chromosomal regions containing C-heterochromatin and fragile sites in the integration of amplified dhfr domains 1989 P. RivaC. De Giuli MorghenL. Larizza Article (author) -
Monosomia del cromosoma 22 e perdita allelica al locus polimorfico c-sis nel meningioma. 1990 P. RivaL. DonedaL. Larizza + Book Part (author) -
Expression of c-sis and c-fos genes in human meningiomas and neurinomas 1992 P. RivaL. Larizza Article (author) -
On the paternal origin of the chromosomes in a 49,XXXXX fetus. 1994 L. VolpiP. RivaL. Larizza + Article (author) -
Satellite DNA sequences flank amplified DHFR domains in marker chromosomes of mouse fibrosarcoma cells 1994 P. RivaL. Larizza + Article (author) -
A 12-bp deletion (7818del12) in the c-kit protooncogene in a large Italian kindred with piebaldism 1995 P. RivaL. Larizza + Article (author) -
Isochromosome 15q of maternal origin in a Prader-Willi patient with pituitary adenoma 1996 P. RivaL. VolpiL. Larizza + Article (author) -
FISH characterization of the Xq21 breakpoint in a translocation carrier with premature ovarian failure 1996 P. RivaI. MagnaniA. M. Fuhrman ContiL. Larizza + Article (author) -
A novel potentially diagnostic polymorphism (4894 A/C) in exon 10 of the human c-kit proto-oncogene 1996 P. RivaL. Larizza Article (author) -
Characterization of a cytogenetic 17q11.2 deletion in an NF1 patient with a contiguous gene syndrome 1996 P. RivaL. DonedaL. Larizza + Article (author) -
Eleven X chromosome breakpoints associated with premature ovarian failure (POF) map to a 15-Mb YAC contig spanning Xq21 1997 P. RivaL. Larizza + Article (author) -
Un metodo rapido e semplice per generare sonde locus-specifiche per l’analisi mediante FISH 1998 P. Riva + Patent -
Chromosomal instability in fibroblasts and mesenchymal tumors from 2 sibs with Rothmund-Thomson syndrome 1998 M. MiozzoP. RivaA. M. Fuhrman ContiL. VolpiL. Larizza + Article (author) -
First cytogenetic study of a recurrent familial chordoma of the clivus 1999 M. MiozzoP. RivaM. VolontèL. LarizzaA. M. Fuhrman Conti + Article (author) -
Mapping of human WHN gene in a 17q11.2 YAC contig and identification of an intragenic STR 1999 L. CorradoP. ColapietroL. LarizzaP. Riva Article (author) -
Distribution and high frequency of novel alleles at NF1 polymorphic markers in the Italian population 1999 P. ColapietroP. RivaL.N. RossiL. Larizza + Article (author) -
Mapping of genes and EST to 17q11.2 to a YAC contig centered on the NF1 gene 2000 P. RivaM. VenturinC. GervasiniL. Larizza + Article (author) -
NF1 microdeletion syndrome: refined FISH characterization of sporadic and familial deletions with locus-specific probes 2000 P. RivaL. CorradoL. Larizza + Article (author) -
19p deletion in recurring leiomyosarcoma lesions from the same patient 2000 P. RivaV. GualandriM. VolontèM. MiozzoA. F. ContiL. Larizza + Article (author) -
A tumor suppressor locus in familial and sporadic chordoma maps to 1p36 2000 M. MiozzoP. RivaM. VolontèF. MacciardiL. LarizzaA. M. Fuhrman Conti + Article (author) -
Mostrati risultati da 1 a 20 di 134
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