Aiello V - Search Results

1

Characterization of a deleted Y chromosome in a male with Turner stigmata.

Calzolari E, Patracchini P, Palazzi P, Aiello V, Ferlini A, Trasforini G, degli Uberti E, Bernardi F. Calzolari E, et al. Among authors: aiello v. Clin Genet. 1993 Jan;43(1):16-22. doi: 10.1111/j.1399-0004.1993.tb04419.x. Clin Genet. 1993. PMID: 8462191

2

Sublocalization of von Willebrand factor pseudogene to 22q11.22-q11.23 by in situ hybridization in a 46,X,t(X;22)(pter;q11.21) translocation.

Patracchini P, Calzolari E, Aiello V, Palazzi P, Banin P, Marchetti G, Bernardi F. Patracchini P, et al. Among authors: aiello v. Hum Genet. 1989 Oct;83(3):264-6. doi: 10.1007/BF00285168. Hum Genet. 1989. PMID: 2793170

3

Sublocalization of the human protein C gene on chromosome 2q13-q14.

Patracchini P, Aiello V, Palazzi P, Calzolari E, Bernardi F. Patracchini P, et al. Among authors: aiello v. Hum Genet. 1989 Jan;81(2):191-2. doi: 10.1007/BF00293902. Hum Genet. 1989. PMID: 2912888

4

New variant of chromosome 11.

Aiello V, Ricci N, Palazzi P, D'Agostino G, Azzini G, Calzolari E. Aiello V, et al. Am J Med Genet. 1994 Apr 15;50(3):294-5. doi: 10.1002/ajmg.1320500314. Am J Med Genet. 1994. PMID: 8042675

5

Characterization and mapping of the 5' portion of von Willebrand factor pseudogene.

Patracchini P, Marchetti G, Aiello V, Croci G, Calzolari E, Bernardi F. Patracchini P, et al. Among authors: aiello v. Hum Genet. 1992 Nov;90(3):297-8. doi: 10.1007/BF00220083. Hum Genet. 1992. PMID: 1487245

6

Cytogenetic and array CGH characterization of an intrachromosomal complex rearrangement of 4q in a patient with a 4q-phenotype.

Sensi A, Prontera P, Buldrini B, Palma S, Aiello V, Gruppioni R, Calzolari E, Volinia S, Martini A. Sensi A, et al. Among authors: aiello v. Am J Med Genet A. 2008 Jan 1;146A(1):110-5. doi: 10.1002/ajmg.a.32059. Am J Med Genet A. 2008. PMID: 18074369

7

Localization of cloned human DNA sequences and analysis of chromosomal alterations by in situ hybridization.

Patracchini P, Aiello V, Marchetti G, Palazzi P, Ferrati M, Calzolari E, Bernardi F. Patracchini P, et al. Among authors: aiello v. Liver. 1992 Aug;12(4 Pt 2):280-5. doi: 10.1111/j.1600-0676.1992.tb01061.x. Liver. 1992. PMID: 1447960

8

Characterization of the pseudogenic and genic homologous regions of von Willebrand factor.

Marchetti G, Patracchini P, Volinia S, Aiello V, Schiavoni M, Ciavarella N, Calzolari E, Schwienbacher C, Bernardi F. Marchetti G, et al. Among authors: aiello v. Br J Haematol. 1991 May;78(1):71-9. doi: 10.1111/j.1365-2141.1991.tb04385.x. Br J Haematol. 1991. PMID: 2043485

9

De novo complex autosomal translocation involving chromosomes 8, 13 and 15 in a girl with a sporadic retinoblastoma.

Calzolari E, Palazzi P, Aiello V, Mazzeo E, Perri P, Minelli A, del Senno L, Patracchini P, Bernardi F. Calzolari E, et al. Among authors: aiello v. Hum Genet. 1987 Sep;77(1):51-4. doi: 10.1007/BF00284713. Hum Genet. 1987. PMID: 3502696

10

Psychiatric disorder in a familial 15;18 translocation and sublocalization of myelin basic protein of 18q22.3.

Calzolari E, Aiello V, Palazzi P, Sensi A, Calzolari S, Orrico D, Calliari L, Holler H, Marzi C, Belli S, Bernardi F, Patracchini P. Calzolari E, et al. Among authors: aiello v. Am J Med Genet. 1996 Apr 9;67(2):154-61. doi: 10.1002/(SICI)1096-8628(19960409)67:2<154::AID-AJMG5>3.0.CO;2-S. Am J Med Genet. 1996. PMID: 8723042

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