Ferrero GB - Search Results

1

The overlap between Sotos and Beckwith-Wiedemann syndromes.

Mussa A, Chiesa N, Porta F, Baldassarre G, Silengo MC, Ferrero GB. Mussa A, et al. Among authors: ferrero gb. J Pediatr. 2010 Jun;156(6):1035-1036. doi: 10.1016/j.jpeds.2010.02.063. Epub 2010 Apr 14. J Pediatr. 2010. PMID: 20394943 No abstract available.

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

Hair anomalies as a sign of mitochondrial disease.

Silengo M, Valenzise M, Spada M, Ferrero GB, Ferraris S, Dassi P, Jarre L. Silengo M, et al. Among authors: ferrero gb. Eur J Pediatr. 2003 Jul;162(7-8):459-461. doi: 10.1007/s00431-003-1228-5. Epub 2003 Apr 24. Eur J Pediatr. 2003. PMID: 12712334

7

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

8

A locus for asphyxiating thoracic dystrophy, ATD, maps to chromosome 15q13.

Morgan NV, Bacchelli C, Gissen P, Morton J, Ferrero GB, Silengo M, Labrune P, Casteels I, Hall C, Cox P, Kelly DA, Trembath RC, Scambler PJ, Maher ER, Goodman FR, Johnson CA. Morgan NV, et al. Among authors: ferrero gb. J Med Genet. 2003 Jun;40(6):431-5. doi: 10.1136/jmg.40.6.431. J Med Genet. 2003. PMID: 12807964 Free PMC article.

9

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

10

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.

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