Larizza L - Search Results

1

Clinical and molecular characterization of Rubinstein-Taybi syndrome patients carrying distinct novel mutations of the EP300 gene.

Negri G, Milani D, Colapietro P, Forzano F, Della Monica M, Rusconi D, Consonni L, Caffi LG, Finelli P, Scarano G, Magnani C, Selicorni A, Spena S, Larizza L, Gervasini C. Negri G, et al. Among authors: larizza l. Clin Genet. 2015 Feb;87(2):148-54. doi: 10.1111/cge.12348. Epub 2014 Feb 17. Clin Genet. 2015. PMID: 24476420

2

FISH analysis in Prader-Willi and Angelman syndrome patients.

Bettio D, Rizzi N, Giardino D, Grugni G, Briscioli V, Selicorni A, Carnevale F, Larizza L. Bettio D, et al. Among authors: larizza l. Am J Med Genet. 1995 Mar 27;56(2):224-8. doi: 10.1002/ajmg.1320560222. Am J Med Genet. 1995. PMID: 7625450

3

FISH characterization of the Xq21 breakpoint in a translocation carrier with premature ovarian failure.

Riva P, Magnani I, Fuhrmann Conti AM, Gelli D, Sala C, Toniolo D, Larizza L. Riva P, et al. Among authors: larizza l. Clin Genet. 1996 Oct;50(4):267-9. doi: 10.1111/j.1399-0004.1996.tb02642.x. Clin Genet. 1996. PMID: 9001815

4

Genotype-phenotype correlation in two sets of monozygotic twins with Williams syndrome.

Castorina P, Selicorni A, Bedeschi F, Dalprà L, Larizza L. Castorina P, et al. Among authors: larizza l. Am J Med Genet. 1997 Mar 3;69(1):107-11. doi: 10.1002/(sici)1096-8628(19970303)69:1<107::aid-ajmg21>3.0.co;2-s. Am J Med Genet. 1997. PMID: 9066894

5

Molecular characterization of FRAXE-positive subjects with mental impairement in two unrelated Italian families.

Russo S, Selicorni A, Bedeschi MF, Natacci F, Viziello P, Fortuna R, Pagani G, Dalprà L, Larizza L. Russo S, et al. Among authors: larizza l. Am J Med Genet. 1998 Jan 23;75(3):304-8. Am J Med Genet. 1998. PMID: 9475603

6

Mapping of human WHN gene in a 17q11.2 YAC contig and identification of an intragenic STR.

Corrado L, Colapietro P, Larizza L, Riva P. Corrado L, et al. Among authors: larizza l. Mol Cell Probes. 1999 Jun;13(3):199-202. doi: 10.1006/mcpr.1999.0237. Mol Cell Probes. 1999. PMID: 10369745

7

Distribution and high frequency of novel alleles at NF1 polymorphic markers in the Italian population.

Natacci F, Colapietro P, Riva P, Corrado L, Rossi LN, Maninetti MM, Casciati MC, Zambrino Ca, Lanzi G, Larizza L. Natacci F, et al. Among authors: larizza l. Mol Cell Probes. 1999 Dec;13(6):415-20. doi: 10.1006/mcpr.1999.0268. Mol Cell Probes. 1999. PMID: 10657145

8

Novel mutations of ubiquitin protein ligase 3A gene in Italian patients with Angelman syndrome.

Russo S, Cogliati F, Viri M, Cavalleri F, Selicorni A, Turolla L, Belli S, Romeo A, Larizza L. Russo S, et al. Among authors: larizza l. Hum Mutat. 2000 Apr;15(4):387. doi: 10.1002/(SICI)1098-1004(200004)15:4<387::AID-HUMU25>3.0.CO;2-W. Hum Mutat. 2000. PMID: 10737998

9

Maternal chromosome 7 hetero/isodisomy in Silver-Russell syndrome and PEG1 biallelic expression.

Russo S, Bedeschi MF, Cogliati F, Natacci F, Gianotti A, Parini R, Selicorni A, Larizza L. Russo S, et al. Among authors: larizza l. Clin Dysmorphol. 2000 Jul;9(3):157-62. doi: 10.1097/00019605-200009030-00001. Clin Dysmorphol. 2000. PMID: 10955473

10

Refined 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.

Finelli P, Giardino D, Russo S, Gottardi G, Cogliati F, Grugni G, Natacci F, Larizza L. Finelli P, et al. Among authors: larizza l. Am J Med Genet. 2001 Apr 1;99(4):308-13. doi: 10.1002/ajmg.1181. Am J Med Genet. 2001. PMID: 11251998

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