Pecile V - Search Results

1

Diagnosis of triploidy in metaphases from uncultured amniocytes.

Pecile V, Demori E, Gambel Benussi D, Dolce S, Amoroso A. Pecile V, et al. Prenat Diagn. 2002 Jan;22(1):78-9. doi: 10.1002/pd.229. Prenat Diagn. 2002. PMID: 11810658 No abstract available.

2

Supernumerary ring chromosome 8: clinical and molecular cytogenetic characterization in a case report.

Demori E, Devescovi R, Benussi DG, Dolce S, Carrozzi M, Villa N, Miertus J, Amoroso A, Pecile V. Demori E, et al. Among authors: pecile v. Am J Med Genet A. 2004 Oct 15;130A(3):288-94. doi: 10.1002/ajmg.a.20677. Am J Med Genet A. 2004. PMID: 15378554 Review.

3

Genomic organization and chromosome mapping of the human homeobox gene HHEX.

Morgutti M, Demori E, Pecile V, Amoroso A, Rustighi A, Manfioletti G. Morgutti M, et al. Among authors: pecile v. Cytogenet Cell Genet. 2001;94(1-2):30-2. doi: 10.1159/000048778. Cytogenet Cell Genet. 2001. PMID: 11701950

4

In situ RT-PCR allows the detection of ornithine decarboxylase mRNA in paraffin embedded archival human hyperplastic breast tissues.

Clerico L, Mancuso T, Da Prato L, Marziliano N, Garagna S, Pecile V, Demori E, Morgutti M, Città A, Parodi S, Amoroso A, Crovella S. Clerico L, et al. Among authors: pecile v. Eur J Histochem. 1999;43(3):179-83. Eur J Histochem. 1999. PMID: 10563250

5

1q44-qter trisomy: clinical report and review of the literature.

Lenzini E, Ballarati L, Drigo P, Carrozzi M, Gambel-Benussi D, Giardino D, Petix V, Rizzotto MR, Pecile V. Lenzini E, et al. Among authors: pecile v. Genet Test Mol Biomarkers. 2009 Feb;13(1):79-86. doi: 10.1089/gtmb.2008.0075. Genet Test Mol Biomarkers. 2009. PMID: 19309278 Review.

6

Genetic mapping of the mouse homologue of the human angiopoietin-1 gene (Agpt) to mouse chromosome 9E2 by in situ hybridization.

Marziliano N, Crovella S, Audero E, Pecile V, Bussolino F, Amoroso A, Garagna S. Marziliano N, et al. Among authors: pecile v. Cytogenet Cell Genet. 1999;87(3-4):199-200. doi: 10.1159/000015466. Cytogenet Cell Genet. 1999. PMID: 10702667 No abstract available.

7

Fragile X syndrome, mental retardation and macroorchidism.

Vatta S, Cigui I, Demori E, Morgutti M, Pecile V, Benussi DG, Serra C, Amoroso A. Vatta S, et al. Among authors: pecile v. Clin Genet. 1998 Oct;54(4):366-7. doi: 10.1034/j.1399-0004.1998.5440420.x. Clin Genet. 1998. PMID: 9831354 No abstract available.

8

Anthracyclines in Nijmegen breakage syndrome.

Barth E, Demori E, Pecile V, Zanazzo GA, Malorgio C, Tamaro P. Barth E, et al. Among authors: pecile v. Med Pediatr Oncol. 2003 Feb;40(2):122-4. doi: 10.1002/mpo.10079. Med Pediatr Oncol. 2003. PMID: 12461799 No abstract available.

9

Chromosome instability and nibrin protein variants in NBS heterozygotes.

Tanzanella C, Antoccia A, Spadoni E, di Masi A, Pecile V, Demori E, Varon R, Marseglia GL, Tiepolo L, Maraschio P. Tanzanella C, et al. Among authors: pecile v. Eur J Hum Genet. 2003 Apr;11(4):297-303. doi: 10.1038/sj.ejhg.5200962. Eur J Hum Genet. 2003. PMID: 12708449

10

Prenatal diagnosis of the fragile-X in male monozygotic twins: discordant expression of the fragile site in amniocytes.

Rocchi M, Pecile V, Archidiacono N, Monni G, Dumez Y, Filippi G. Rocchi M, et al. Among authors: pecile v. Prenat Diagn. 1985 May-Jun;5(3):229-31. doi: 10.1002/pd.1970050311. Prenat Diagn. 1985. PMID: 4022944

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