Larizza L - Search Results

1

Cryptic subtelomeric translocation t(2;16)(q37;q24) segregating in a family with unexplained stillbirths and a dysmorphic, slightly retarded child.

Giardino D, Finelli P, Gottardi G, Clerici D, Mosca F, Briscioli V, Larizza L. Giardino D, et al. Among authors: larizza l. Eur J Hum Genet. 2001 Dec;9(12):881-6. doi: 10.1038/sj.ejhg.5200730. Eur J Hum Genet. 2001. PMID: 11840188 Free article.

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

Isochromosome 15q of maternal origin in a Prader-Willi patient with pituitary adenoma.

Bettio D, Giardino D, Rizzi N, Riva P, Volpi L, Barantani E, Tagliaferri A, Larizza L. Bettio D, et al. Among authors: larizza l. Acta Genet Med Gemellol (Roma). 1996;45(1-2):213-6. doi: 10.1017/s000156600000132x. Acta Genet Med Gemellol (Roma). 1996. PMID: 8872033

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

Cytogenetic study of pituitary adenomas.

Bettio D, Rizzi N, Giardino D, Persani L, Pecori-Giraldi F, Losa M, Larizza L. Bettio D, et al. Among authors: larizza l. Cancer Genet Cytogenet. 1997 Oct 15;98(2):131-6. doi: 10.1016/s0165-4608(96)00426-8. Cancer Genet Cytogenet. 1997. PMID: 9332478

6

Translocation (7;17)(q22;p13) as a sole karyotypic change in an adrenal adenoma.

Bettio D, Rizzi N, Giardino D, Virduci T, Loli P, Larizza L. Bettio D, et al. Among authors: larizza l. Cancer Genet Cytogenet. 1998 Jun;103(2):180-1. doi: 10.1016/s0165-4608(97)00389-0. Cancer Genet Cytogenet. 1998. PMID: 9614923 No abstract available.

7

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

8

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

9

NF1 microdeletion syndrome: refined FISH characterization of sporadic and familial deletions with locus-specific probes.

Riva P, Corrado L, Natacci F, Castorina P, Wu BL, Schneider GH, Clementi M, Tenconi R, Korf BR, Larizza L. Riva P, et al. Among authors: larizza l. Am J Hum Genet. 2000 Jan;66(1):100-9. doi: 10.1086/302709. Am J Hum Genet. 2000. PMID: 10631140 Free PMC article.

10

Non-random trisomies of chromosomes 5, 8 and 12 in the prolactinoma sub-type of pituitary adenomas: conventional cytogenetics and interphase FISH study.

Finelli P, Giardino D, Rizzi N, Buiatiotis S, Virduci T, Franzin A, Losa M, Larizza L. Finelli P, et al. Among authors: larizza l. Int J Cancer. 2000 May 1;86(3):344-50. doi: 10.1002/(sici)1097-0215(20000501)86:3<344::aid-ijc7>3.0.co;2-8. Int J Cancer. 2000. PMID: 10760821 Free article.

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