Pecile V - Search Results

1

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.

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

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

5

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.

6

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.

7

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

8

Ophthalmic features in a dysmorphic boy with chromosome 4q deletion and duplication.

Parentin F, Fabretto A, Benussi DG, Petix V, Marchetti F, Dalprà L, Redaelli S, Pensiero S, Pecile V. Parentin F, et al. Among authors: pecile v. Ophthalmic Genet. 2009 Jun;30(2):103-5. doi: 10.1080/13816810802592559. Ophthalmic Genet. 2009. PMID: 19373683

9

De novo 6.9 Mb interstitial deletion on chromosome 4q31.1-q32.1 in a girl with severe speech delay and dysmorphic features.

Fabretto A, Santa Rocca M, Perrone MD, Skabar A, Pecile V, Gasparini P. Fabretto A, et al. Among authors: pecile v. Am J Med Genet A. 2012 Apr;158A(4):882-7. doi: 10.1002/ajmg.a.35239. Epub 2012 Mar 9. Am J Med Genet A. 2012. PMID: 22407795

10

Screening for fetal anomalies by ultrasound at 14 and 21 weeks.

D'Ottavio G, Meir YJ, Rustico MA, Pecile V, Fischer-Tamaro L, Conoscenti G, Natale R, Mandruzzato GP. D'Ottavio G, et al. Among authors: pecile v. Ultrasound Obstet Gynecol. 1997 Dec;10(6):375-80. doi: 10.1046/j.1469-0705.1997.10060375.x. Ultrasound Obstet Gynecol. 1997. PMID: 9476319 Free article.

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