Larizza L - Search Results

1

RNA processing defects of the helicase gene RECQL4 in a compound heterozygous Rothmund-Thomson patient.

Beghini A, Castorina P, Roversi G, Modiano P, Larizza L. Beghini A, et al. Among authors: larizza l. Am J Med Genet A. 2003 Jul 30;120A(3):395-9. doi: 10.1002/ajmg.a.20154. Am J Med Genet A. 2003. PMID: 12838562

2

Microsatellite instability in IVS3 of murine c-fes gene: tumor-associated rearrangement and mammalian divergence.

Volpi L, Beghini A, Rossi D, Larizza L. Volpi L, et al. Among authors: larizza l. Mamm Genome. 1996 Sep;7(9):682-5. doi: 10.1007/s003359900205. Mamm Genome. 1996. PMID: 8703122

3

Characterization of a cytogenetic 17q11.2 deletion in an NF1 patient with a contiguous gene syndrome.

Riva P, Castorina P, Manoukian S, Dalprà L, Doneda L, Marini G, den Dunnen J, Larizza L. Riva P, et al. Among authors: larizza l. Hum Genet. 1996 Dec;98(6):646-50. doi: 10.1007/s004390050277. Hum Genet. 1996. PMID: 8931693

4

FISH characterization of small supernumerary marker chromosomes in two Prader-Willi patients.

Bettio D, Rizzi N, Giardino D, Gurrieri F, Silvestri G, Grugni G, Larizza L. Bettio D, et al. Among authors: larizza l. Am J Med Genet. 1997 Jan 10;68(1):99-104. doi: 10.1002/(sici)1096-8628(19970110)68:1<99::aid-ajmg21>3.0.co;2-i. Am J Med Genet. 1997. PMID: 8986287

5

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

6

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

7

Chromosomal instability in fibroblasts and mesenchymal tumors from 2 sibs with Rothmund-Thomson syndrome.

Miozzo M, Castorina P, Riva P, Dalprà L, Fuhrman Conti AM, Volpi L, Hoe TS, Khoo A, Wiegant J, Rosenberg C, Larizza L. Miozzo M, et al. Among authors: larizza l. Int J Cancer. 1998 Aug 12;77(4):504-10. doi: 10.1002/(sici)1097-0215(19980812)77:4<504::aid-ijc5>3.0.co;2-y. Int J Cancer. 1998. PMID: 9679749

8

In vivo differentiation of mast cells from acute myeloid leukemia blasts carrying a novel activating ligand-independent C-kit mutation.

Beghini A, Cairoli R, Morra E, Larizza L. Beghini A, et al. Among authors: larizza l. Blood Cells Mol Dis. 1998 Jun;24(2):262-70. doi: 10.1006/bcmd.1998.0191. Blood Cells Mol Dis. 1998. PMID: 9714703

9

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

10

FISH characterization of two supernumerary r(1) associated with distinct clinical phenotypes.

Giardino D, Bettio D, Gottardi G, Rizzi N, Pierluigi M, Perfumo C, Calì A, Dagna Bricarelli F, Larizza L. Giardino D, et al. Among authors: larizza l. Am J Med Genet. 1999 Jun 4;84(4):377-80. Am J Med Genet. 1999. PMID: 10340656

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