Ferrero GB - Search Results

1

Inherited and Sporadic Epimutations at the IGF2-H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumor.

Riccio A, Sparago A, Verde G, De Crescenzo A, Citro V, Cubellis MV, Ferrero GB, Silengo MC, Russo S, Larizza L, Cerrato F. Riccio A, et al. Among authors: ferrero gb. Endocr Dev. 2009;14:1-9. doi: 10.1159/000207461. Epub 2009 Feb 27. Endocr Dev. 2009. PMID: 19293570 Review.

2

Hair as a diagnostic tool in dysmorphology.

Silengo M, Valenzise M, Sorasio L, Ferrero GB. Silengo M, et al. Among authors: ferrero gb. Clin Genet. 2002 Oct;62(4):270-2. doi: 10.1034/j.1399-0004.2002.620403.x. Clin Genet. 2002. PMID: 12372052

3

A possible relationship between Beckwith-Wiedemann syndrome and prune belly syndrome.

Silengo M, Barberis L, Ferrero GB, Sorasio L, Valenzise M. Silengo M, et al. Among authors: ferrero gb. Clin Dysmorphol. 2002 Oct;11(4):293-4. doi: 10.1097/00019605-200210000-00012. Clin Dysmorphol. 2002. PMID: 12401997

4

Oral, facial, digital, vertebral anomalies with psychomotor delay: a mild form of OFD type Gabrielli?

Ferrero GB, Valenzise M, Franco B, Defilippi C, Gregato G, Corsello G, Pepe E, Silengo M. Ferrero GB, et al. Am J Med Genet. 2002 Dec 1;113(3):291-4. doi: 10.1002/ajmg.10815. Am J Med Genet. 2002. PMID: 12439899

5

Mental retardation, peculiar facial dysmorphism and HbH inclusions in a 4-year-old boy.

Valenzise M, Ferrero GB, Tosi MT, Ferraris S, Silengo M. Valenzise M, et al. Among authors: ferrero gb. Eur J Pediatr. 2002 Nov;161(11):627-8. doi: 10.1007/s00431-002-1049-y. Eur J Pediatr. 2002. PMID: 12532943 No abstract available.

6

Subcortical band heterotopia with simplified gyral pattern and syndactyly.

Sicca F, Silengo M, Parrini E, Ferrero GB, Guerrini R. Sicca F, et al. Among authors: ferrero gb. Am J Med Genet A. 2003 Jun 1;119A(2):207-10. doi: 10.1002/ajmg.a.20111. Am J Med Genet A. 2003. PMID: 12749065

7

Malformations following methimazole exposure in utero: an open issue.

Ferraris S, Valenzise M, Lerone M, Divizia MT, Rosaia L, Blaid D, Nemelka O, Ferrero GB, Silengo M. Ferraris S, et al. Among authors: ferrero gb. Birth Defects Res A Clin Mol Teratol. 2003 Dec;67(12):989-92. doi: 10.1002/bdra.10098. Birth Defects Res A Clin Mol Teratol. 2003. PMID: 14745920

8

Pachygyria and cerebellar hypoplasia in a patient with a 2q22-q23 deletion that includes the ZFHX1B gene.

Silengo M, Ferrero GB, Wakamatsu N. Silengo M, et al. Among authors: ferrero gb. Am J Med Genet A. 2004 May 15;127A(1):109. doi: 10.1002/ajmg.a.20607. Am J Med Genet A. 2004. PMID: 15103730 No abstract available.

9

Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith-Wiedemann syndrome.

Sparago A, Cerrato F, Vernucci M, Ferrero GB, Silengo MC, Riccio A. Sparago A, et al. Among authors: ferrero gb. Nat Genet. 2004 Sep;36(9):958-60. doi: 10.1038/ng1410. Epub 2004 Aug 15. Nat Genet. 2004. PMID: 15314640

10

Phenotype resembling Donnai-Barrow syndrome in a patient with 9qter;16qter unbalanced translocation.

Ferrero GB, Belligni E, Sorasio L, Delmonaco AG, Oggero R, Faravelli F, Pierluigi M, Silengo M. Ferrero GB, et al. Am J Med Genet A. 2006 Apr 15;140(8):892-4. doi: 10.1002/ajmg.a.31188. Am J Med Genet A. 2006. PMID: 16532464

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

196 results

Search Page