Larizza L - Search Results

1

Somatic mosaicism in Cornelia de Lange syndrome: a further contributor to the wide clinical expressivity?

Castronovo P, Delahaye-Duriez A, Gervasini C, Azzollini J, Minier F, Russo S, Masciadri M, Selicorni A, Verloes A, Larizza L. Castronovo P, et al. Among authors: larizza l. Clin Genet. 2010 Dec;78(6):560-4. doi: 10.1111/j.1399-0004.2010.01408.x. Clin Genet. 2010. PMID: 20331678

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

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

4

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

5

An unusual fragile X sibship: female compound heterozygote and male with a partially methylated full mutation.

Russo S, Briscioli V, Cogliati F, Macchi M, Lalatta F, Larizza L. Russo S, et al. Among authors: larizza l. Clin Genet. 1998 Oct;54(4):309-14. doi: 10.1034/j.1399-0004.1998.5440408.x. Clin Genet. 1998. PMID: 9831342

6

New case of the Richieri-Costa/Guion-Almeida syndrome.

Natacci F, Pierri M, Rossetti M, Sala M, Larizza L. Natacci F, et al. Among authors: larizza l. Am J Med Genet. 1999 Apr 23;83(5):419-21. doi: 10.1002/(sici)1096-8628(19990423)83:5<419::aid-ajmg15>3.0.co;2-l. Am J Med Genet. 1999. PMID: 10232755

7

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

8

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

9

Mapping to distal Xq28 of nonspecific X-linked mental retardation MRX72: linkage analysis and clinical findings in a three-generation Sardinian family.

Russo S, Cogliati F, Cavalleri F, Cassitto MG, Giglioli R, Toniolo D, Casari G, Larizza L. Russo S, et al. Among authors: larizza l. Am J Med Genet. 2000 Oct 23;94(5):376-82. doi: 10.1002/1096-8628(20001023)94:5<376::aid-ajmg6>3.0.co;2-a. Am J Med Genet. 2000. PMID: 11050621

10

Patient with large 17p11.2 deletion presenting with Smith-Magenis syndrome and Joubert syndrome phenotype.

Natacci F, Corrado L, Pierri M, Rossetti M, Zuccarini C, Riva P, Miozzo M, Larizza L. Natacci F, et al. Among authors: larizza l. Am J Med Genet. 2000 Dec 18;95(5):467-72. doi: 10.1002/1096-8628(20001218)95:5<467::aid-ajmg11>3.0.co;2-t. Am J Med Genet. 2000. PMID: 11146468

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