Ferrero GB - Search Results

1

A novel 3q29 deletion associated with autism, intellectual disability, psychiatric disorders, and obesity.

Biamino E, Di Gregorio E, Belligni EF, Keller R, Riberi E, Gandione M, Calcia A, Mancini C, Giorgio E, Cavalieri S, Pappi P, Talarico F, Fea AM, De Rubeis S, Cirillo Silengo M, Ferrero GB, Brusco A. Biamino E, et al. Among authors: ferrero gb. Am J Med Genet B Neuropsychiatr Genet. 2016 Mar;171B(2):290-9. doi: 10.1002/ajmg.b.32406. Epub 2015 Dec 1. Am J Med Genet B Neuropsychiatr Genet. 2016. PMID: 26620927 Free article.

2

Myhre's syndrome in a girl with normal intelligence.

Rulli I, Ferrero GB, Belligni E, Delmonaco AG, Defilippi C, Silengo M. Rulli I, et al. Among authors: ferrero gb. Am J Med Genet A. 2005 Apr 1;134A(1):100-2. doi: 10.1002/ajmg.a.30444. Am J Med Genet A. 2005. PMID: 15723310 No abstract available.

3

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

4

AEC syndrome: further evidence of a common genetic etiology with Rapp-Hodgkin syndrome.

Sorasio L, Ferrero GB, Garelli E, Brunello G, Martano C, Carando A, Belligni E, Dianzani I, Cirillo Silengo M. Sorasio L, et al. Among authors: ferrero gb. Eur J Med Genet. 2006 Nov-Dec;49(6):520-2. doi: 10.1016/j.ejmg.2006.05.003. Epub 2006 Jun 30. Eur J Med Genet. 2006. PMID: 16824815 No abstract available.

5

Presenting phenotype and clinical evaluation in a cohort of 22 Williams-Beuren syndrome patients.

Ferrero GB, Biamino E, Sorasio L, Banaudi E, Peruzzi L, Forzano S, di Cantogno LV, Silengo MC. Ferrero GB, et al. Eur J Med Genet. 2007 Sep-Oct;50(5):327-37. doi: 10.1016/j.ejmg.2007.05.005. Epub 2007 Jun 6. Eur J Med Genet. 2007. PMID: 17625998

6

Clinical and molecular characterization of 40 patients with Noonan syndrome.

Ferrero GB, Baldassarre G, Delmonaco AG, Biamino E, Banaudi E, Carta C, Rossi C, Silengo MC. Ferrero GB, et al. Eur J Med Genet. 2008 Nov-Dec;51(6):566-72. doi: 10.1016/j.ejmg.2008.06.011. Epub 2008 Jul 17. Eur J Med Genet. 2008. PMID: 18678287

7

Subtelomeric FISH analysis in 76 patients with syndromic developmental delay/intellectual disability.

Belligni EF, Biamino E, Molinatto C, Messa J, Pierluigi M, Faravelli F, Zuffardi O, Ferrero GB, Silengo MC. Belligni EF, et al. Among authors: ferrero gb. Ital J Pediatr. 2009 Apr 27;35(1):9. doi: 10.1186/1824-7288-35-9. Ital J Pediatr. 2009. PMID: 19490664 Free PMC article.

8

An atypical 7q11.23 deletion in a normal IQ Williams-Beuren syndrome patient.

Ferrero GB, Howald C, Micale L, Biamino E, Augello B, Fusco C, Turturo MG, Forzano S, Reymond A, Merla G. Ferrero GB, et al. Eur J Hum Genet. 2010 Jan;18(1):33-8. doi: 10.1038/ejhg.2009.108. Eur J Hum Genet. 2010. PMID: 19568270 Free PMC article.

9

A novel H208D TP63 mutation in a familial case of ectrodactyly-ectodermal dysplasia-cleft lip/palate syndrome without clefting.

Sorasio L, Biamino E, Garelli E, Ferrero GB, Silengo MC. Sorasio L, et al. Among authors: ferrero gb. Clin Exp Dermatol. 2009 Dec;34(8):e726-8. doi: 10.1111/j.1365-2230.2009.03451.x. Epub 2009 Jul 29. Clin Exp Dermatol. 2009. PMID: 19663851

10

Eyebrow anomalies as a diagnostic sign of genomic disorders.

Silengo M, Belligni E, Molinatto C, Baldassarre G, Biamino E, Chiesa N, Zuffardi O, Girirajan S, Eichler EE, Ferrero GB. Silengo M, et al. Among authors: ferrero gb. Clin Genet. 2010 Jan;77(1):28-31. doi: 10.1111/j.1399-0004.2009.01347.x. Clin Genet. 2010. PMID: 20092588

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 Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

209 results

Search Page

Filters