LARIZZA, LIDIA

LARIZZA, LIDIA  

Dipartimento di Scienze della Salute  

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Risultati 1 - 20 di 298 (tempo di esecuzione: 0.007 secondi).
Titolo Data di pubblicazione Autore(i) Tipo File Abstract
13q deletion and CNS anomalies : further insights from karyotype-phenotype analyses of 14 patients 1-gen-2007 P. FinelliL. Larizza + Article (author) -
13q mosaic deletion including RB1 associated to mild phenotype and no cancer outcome-case report and review of the literature 1-set-2018 Bestetti I.Sironi A.Catusi I.Mariani M.Larizza L.Castronovo C.Finelli P. + Article (author) -
19p deletion in recurring leiomyosarcoma lesions from the same patient 1-giu-2000 P. RivaV. GualandriM. VolontèM. MiozzoA. F. ContiL. Larizza + Article (author) -
7p22.1 microduplication syndrome : clinical and molecular characterization of an adult case and review of the literature 1-nov-2015 A. VignoliA. PeronM.P. RecalcatiI. CatusiL. Larizza + Article (author) -
9q34.3 microduplications lead to neurodevelopmental disorders through EHMT1 overexpression 1-ago-2019 Castronovo CSironi AZimbalatti DBestetti ICrippa MLarizza LFinelli P. + Article (author) -
A 12-bp deletion (7818del12) in the c-kit protooncogene in a large Italian kindred with piebaldism 1-gen-1995 P. RivaL. Larizza + Article (author) -
A 12.4 Mb duplication of 17q11.2q12 in a patient with psychomotor developmental delay and minor anomalies 1-gen-2010 D. MilaniS. MaitzL. Larizza + Article (author) -
A comparative analysis of collagen III, IV, laminin and fibronectin in Duchenne muscular dystrophy biopsies and cell cultures 1-ott-1986 G. MeolaA. M. ContiL. Larizza + Article (author) -
A family with three sibs carrying trisomy 21 1-mag-1975 G. SimoniL. Larizza + Article (author) -
A fluorescent method for detecting low-grade 11patUPD mosaicism in Beckwith-Wiedemann syndrome 1-gen-1986 MENCARELLI, MONICAL. Larizza + Article (author) -
A novel mosaic NSD1 intragenic deletion in a patient with an atypical phenotype 1-mar-2013 D. RusconiM. CrippaC. GervasiniL. LarizzaP. Finelli + Article (author) -
A novel mutation (Gln266-->His) in the alpha 1 subunit of the inhibitory glycine-receptor gene (GLRA1) in hereditary hyperekplexia 1-feb-1996 L. Larizza + Article (author) -
A novel potentially diagnostic polymorphism (4894 A/C) in exon 10 of the human c-kit proto-oncogene 1-ott-1996 P. RivaL. Larizza Article (author) -
A rare chromosome 5 heterochromatic variant derived from insertion of 9qh satellite 3 sequences 1-ago-1998 L. DonedaL. Larizza + Article (author) -
Acquisition of high metastatic capacity after in vitro fusion of a nonmetastatic tumor line with a bone marrow-derived macrophage 1-nov-1984 L. Larizza + Article (author) -
Activation of c-fos and c-fes in metastatic lympho-macrophage hybrids 30-set-1992 L. VolpiL. Larizza + Article (author) -
Activation of cyclophosphamide by freeze-dried microsomes as an in vitro test of cytogenetic damage 1-dic-1982 E. DolfiniL. LarizzaA. M. Fuhrman Conti + Article (author) -
AML with t(8;21) and trisomy 4: possible involvement of c-kit? 1-set-2003 A. BeghiniL. Larizza + Article (author) -
Amplification of a novel c-Kit activating mutation Asn(822)-Lys in the Kasumi-1 cell line: a t(8;21)-Kit mutant model for acute myeloid leukemia 1-gen-2002 A. BeghiniI. MagnaniL. Larizza + Article (author) -
An improved procedure for in situ RTPCR 1-feb-1996 L. VolpiL. DonedaM. G. GrimoldiL. Larizza + Article (author) -