Romano V - Search Results

1

Autosomal microsatellite and mtDNA genetic analysis in Sicily (Italy).

Romano V, Calì F, Ragalmuto A, D'Anna RP, Flugy A, De Leo G, Giambalvo O, Lisa A, Fiorani O, Di Gaetano C, Salerno A, Tamouza R, Charron D, Zei G, Matullo G, Piazza A. Romano V, et al. Ann Hum Genet. 2003 Jan;67(Pt 1):42-53. doi: 10.1046/j.1469-1809.2003.00007.x. Ann Hum Genet. 2003. PMID: 12556234

2

The STR252-IVS10nt546-VNTR7 phenylalanine hydroxylase minihaplotype in five Mediterranean samples.

Calì F, Dianzani I, Desviat LR, Perez B, Ugarte M, Ozguc M, Seyrantepe V, Shiloh Y, Giannattasio S, Carducci C, Bosco P, De Leo G, Piazza A, Romano V. Calì F, et al. Among authors: romano v. Hum Genet. 1997 Sep;100(3-4):350-5. doi: 10.1007/s004390050515. Hum Genet. 1997. PMID: 9272154

3

MtDNA control region and RFLP data for Sicily and France.

Cali F, Le Roux MG, D'Anna R, Flugy A, De Leo G, Chiavetta V, Ayala GF, Romano V. Cali F, et al. Among authors: romano v. Int J Legal Med. 2001;114(4-5):229-31. doi: 10.1007/s004140000169. Int J Legal Med. 2001. PMID: 11355400

4

A methodological strategy for PAH genotyping in populations with a marked molecular heterogeneity of hyperphenylalaninemia.

Romano V, Lio D, Calì F, Scola L, Leggio L, D'Anna C, DeLeo G, Salermo A. Romano V, et al. Mol Cell Probes. 2001 Feb;15(1):13-9. doi: 10.1006/mcpr.2000.0330. Mol Cell Probes. 2001. PMID: 11284432

5

Genetic heterogeneity in five Italian regions: analysis of PAH mutations and minihaplotypes.

Giannattasio S, Dianzani I, Lattanzio P, Spada M, Romano V, Calì F, Andria G, Ponzone A, Marra E, Piazza A. Giannattasio S, et al. Among authors: romano v. Hum Hered. 2001;52(3):154-9. doi: 10.1159/000053371. Hum Hered. 2001. PMID: 11588399

6

PAH gene mutations in the Sicilian population: association with minihaplotypes and expression analysis.

Mirisola MG, Cali F, Gloria A, Schinocca P, D'Amato M, Cassara G, Leo GD, Palillo L, Meli C, Romano V. Mirisola MG, et al. Among authors: romano v. Mol Genet Metab. 2001 Nov;74(3):353-61. doi: 10.1006/mgme.2001.3211. Mol Genet Metab. 2001. PMID: 11708866

7

Y-chromosomal STR haplotypes in Sicily.

Robino C, Inturri S, Gino S, Torre C, Di Gaetano C, Crobu F, Romano V, Matullo G, Piazza A. Robino C, et al. Among authors: romano v. Forensic Sci Int. 2006 Jun 2;159(2-3):235-40. doi: 10.1016/j.forsciint.2005.05.015. Epub 2005 Jun 28. Forensic Sci Int. 2006. PMID: 15990263

8

Two novel PAH gene mutations detected in Italian phenylketonuric patients.

Argiolas A, Bosco P, Calì F, Ceratto N, Anello G, Riva E, Biasucci G, Carducci C, Romano V. Argiolas A, et al. Among authors: romano v. Hum Genet. 1997 Feb;99(2):275-8. doi: 10.1007/s004390050353. Hum Genet. 1997. PMID: 9048935

9

Analysis of the gastrin-releasing peptide receptor gene in Italian patients with autism spectrum disorders.

Seidita G, Mirisola M, D'Anna RP, Gallo A, Jensen RT, Mantey SA, Gonzalez N, Falco M, Zingale M, Elia M, Cucina L, Chiavetta V, Romano V, Cali F. Seidita G, et al. Among authors: romano v. Am J Med Genet B Neuropsychiatr Genet. 2008 Sep 5;147B(6):807-13. doi: 10.1002/ajmg.b.30752. Am J Med Genet B Neuropsychiatr Genet. 2008. PMID: 18393381 Free article.

10

Association between haplotypes, hind III-VNTR alleles and mutations at the PAH locus in Sicily.

Romano V, Calì F, Guldberg P, Güttler F, Indelicato A, Bosco P, Ceratto N. Romano V, et al. Acta Paediatr Suppl. 1994 Dec;407:39-40. doi: 10.1111/j.1651-2227.1994.tb13446.x. Acta Paediatr Suppl. 1994. PMID: 7766953

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