Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

92 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Cloverleaf skull anomaly and de novo trisomy 4p.
de Brasi D, Perone L, di Micco P, Andria G, Sebastio G, Iaccarino E, Pinto L, Aliberti F. de Brasi D, et al. Among authors: sebastio g. J Med Genet. 1999 May;36(5):422-4. J Med Genet. 1999. PMID: 10353793 Free PMC article. No abstract available.
Molecular and cytogenetic characterization of a recurrent unbalanced translocation (4;21)(p16.3;q22.1): relevance to the Wolf-Hirschhorn and Down syndrome critical regions.
Sebastio G, Perone L, Guzzetta V, Sebastio L, Vicari L, Della Casa R, Gurrieri F, Zappata S, Pomponi MG, Mazzei A, Neri G, Andria G, Brahe C. Sebastio G, et al. Among authors: sebastio l. Am J Med Genet. 1996 May 17;63(2):366-72. doi: 10.1002/(SICI)1096-8628(19960517)63:2<366::AID-AJMG8>3.0.CO;2-R. Am J Med Genet. 1996. PMID: 8725787
Severe cardiac anomalies in sibs with Larsen syndrome.
Strisciuglio P, Sebastio G, Andria G, Maione S, Raia V. Strisciuglio P, et al. Among authors: sebastio g. J Med Genet. 1983 Dec;20(6):422-4. doi: 10.1136/jmg.20.6.422. J Med Genet. 1983. PMID: 6655668 Free PMC article.
A new patient with Lowry-Wood syndrome with mild phenotype.
Brunetti-Pierri N, De Brasi D, Ikegawa S, Camera G, Andria G, Sebastio G. Brunetti-Pierri N, et al. Among authors: sebastio g. Am J Med Genet A. 2003 Apr 1;118A(1):68-70. doi: 10.1002/ajmg.a.20008. Am J Med Genet A. 2003. PMID: 12605445
Trisomy 18 and hypertrophy cardiomyopathy in an 18-year-old woman.
Limongelli G, Pacileo G, Melis D, Calabro' P, Digilio MC, Sarkozy A, Maddaloni V, Capozzi G, Sebastio G, Andria G, Calabro' R. Limongelli G, et al. Among authors: sebastio g. Am J Med Genet A. 2008 Feb 1;146A(3):327-9. doi: 10.1002/ajmg.a.32149. Am J Med Genet A. 2008. PMID: 18203191 No abstract available.
Case of Myhre syndrome with autism and peculiar skin histological findings.
Titomanlio L, Marzano MG, Rossi E, D'Armiento M, De Brasi D, Vega GR, Andreucci MV, Orsini AV, Santoro L, Sebastio G. Titomanlio L, et al. Among authors: sebastio g. Am J Med Genet. 2001 Oct 1;103(2):163-5. doi: 10.1002/ajmg.1517. Am J Med Genet. 2001. PMID: 11568925
92 results