Sfoglia per Autore  

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Mostrati risultati da 21 a 40 di 179
Titolo Data di pubblicazione Autori Tipo File Abstract
Somatic genetic changes in lung cancer and precancerous lesions 1995 M. Miozzo + Article (author) -
Involvement of chromosomes 17 and 22 in dermatofibrosarcoma protuberans 1995 M. Miozzo + Article (author) -
Genetic Evidence for an Independent Origin of Multiple Preneoplastic and Neoplastic Lung Lesions 1995 M. MiozzoDE GREGORIO, LAURA + Article (author) -
Mapping of a putative tumor suppressor locus to proximal 7p in Wilms tumors 1996 M. Miozzo + Article (author) -
Microsatellite alterations in bronchial and sputum specimens of lung cancer patients 1996 M. Miozzo + Article (author) -
Relevance of cytogenetic and fluorescent in situ hybridization analyses in the clinical assessment of soft tissue sarcoma 1997 M. Miozzo + Article (author) -
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) -
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) -
Patient with large 17p11.2 deletion presenting with Smith-Magenis syndrome and Joubert syndrome phenotype 2000 L. CorradoP. RivaM. MiozzoL. Larizza + Article (author) -
Post-zygotic origin of complete maternal chromosome 7 isodysomy and consequent loss of placental PEG1/MEST expression 2001 M. MiozzoT. RadaelliT. PersicoE. FerrazziI. CetinG. PardiG. Simoni + Article (author) -
Relationship between clinical and genetic features in inverted duplicated chromosome 15 patients 2001 M. Miozzo + Article (author) -
Post-zygotic origin of complete maternal chromosome 7 isodisomy and consequent loss of placental PEG1/MEST expression 2001 M. MiozzoF. R. GratiG. BulfamanteT. RadaelliT. PersicoI. CetinG. Pardi + Article (author) -
A patient defines the interstitial 1q deletion syndrome characterized by antithrombin III deficiency 2001 M. Miozzo + Article (author) -
The role of imprinted genes in fetal growth 2002 M. MiozzoG. Simoni Article (author) -
HER-2/Neu alterations in non-small cell lung cancer: a comprehensive evaluation by real time reverse transcription-PCR, fluorescence in situ hybridization and immunohistochemistry 2003 M. FalleniM. MiozzoM. RoncalliG. CoggiS. Bosari + Article (author) -
Mapping of candidate region for chordoma development to 1p36.13 by LOH analysis 2003 P. RivaORZAN, FRANCESCAA.M. Fuhrman ContiM. MiozzoL. Larizza + Article (author) -
Frequency of monosomy X in women with primary biliary cirrhosis 2004 P. InvernizziM. MiozzoP.M. BattezzatiF.R. GratiG. SimoniC. SelmiM. Podda + Article (author) -
Biparental expression of ESX1L gene in placentas from normal and intrauterine growth-restricted pregnancies 2004 F.R. GratiS.M. SirchiaB. GentilinF. RossellaL. RamoscelliG. BulfamanteI. CetinG. SimoniM. Miozzo + Article (author) -
Mostrati risultati da 21 a 40 di 179
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