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

314 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Fontaine-Farriaux craniosynostosis: second report in the literature.
Priolo M, De Toni T, Baffico M, Cama A, Seri M, Cusano R, Costabello L, Fondelli P, Capra V, Silengo M, Ravazzolo R, Lerone M. Priolo M, et al. Among authors: seri m. Am J Med Genet. 2001 May 1;100(3):214-8. Am J Med Genet. 2001. PMID: 11343306
RET mutations in exons 13 and 14 of FMTC patients.
Bolino A, Schuffenecker I, Luo Y, Seri M, Silengo M, Tocco T, Chabrier G, Houdent C, Murat A, Schlumberger M, et al. Bolino A, et al. Among authors: seri m. Oncogene. 1995 Jun 15;10(12):2415-9. Oncogene. 1995. PMID: 7784092
Inheritance of Niikawa-Kuroki (Kabuki makeup) syndrome.
Silengo M, Lerone M, Seri M, Romeo G. Silengo M, et al. Among authors: seri m. Am J Med Genet. 1996 Dec 18;66(3):368. doi: 10.1002/(SICI)1096-8628(19961218)66:3<368::AID-AJMG28>3.0.CO;2-J. Am J Med Genet. 1996. PMID: 8985504 No abstract available.
Frequency of RET mutations in long- and short-segment Hirschsprung disease.
Seri M, Yin L, Barone V, Bolino A, Celli I, Bocciardi R, Pasini B, Ceccherini I, Lerone M, Kristoffersson U, Larsson LT, Casasa JM, Cass DT, Abramowicz MJ, Vanderwinden JM, Kravcenkiene I, Baric I, Silengo M, Martucciello G, Romeo G. Seri M, et al. Hum Mutat. 1997;9(3):243-9. doi: 10.1002/(SICI)1098-1004(1997)9:3<243::AID-HUMU5>3.0.CO;2-8. Hum Mutat. 1997. PMID: 9090527
Association of multiple endocrine neoplasia type 2 and Hirschsprung disease.
Romeo G, Ceccherini I, Celli J, Priolo M, Betsos N, Bonardi G, Seri M, Yin L, Lerone M, Jasonni V, Martucciello G. Romeo G, et al. Among authors: seri m. J Intern Med. 1998 Jun;243(6):515-20. doi: 10.1046/j.1365-2796.1998.00332.x. J Intern Med. 1998. PMID: 9681852 Free article.
A new candidate region for the positional cloning of the XLP gene.
Bolino A, Yin L, Seri M, Cusano R, Cinti R, Coffey A, Brooksbank R, Howell G, Bentley D, Davis JR, Lanyi A, Huang D, Stark M, Creaven M, Bjørkhaug L, Heitzmann F, Lamartine J, Gaudi S, Sylla BS, Lenoir GM, Castagnola E, Giacchino R, Porta G, Franco B, Zollo M, Sumegi J, Romeo G. Bolino A, et al. Among authors: seri m. Eur J Hum Genet. 1998 Sep-Oct;6(5):509-17. doi: 10.1038/sj.ejhg.5200249. Eur J Hum Genet. 1998. PMID: 9801876
314 results