Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Text availability
Article attribute
Article type
Publication date

Search Results

34 results
Filters applied: . Clear all Results are displayed in a computed author sort order. Results by year timeline is unavailable
Page 1
Cytogenetic and molecular evaluation of 241 small supernumerary marker chromosomes: cooperative study of 19 Italian laboratories.
Dalprà L, Giardino D, Finelli P, Corti C, Valtorta C, Guerneri S, Ilardi P, Fortuna R, Coviello D, Nocera G, Amico FP, Martinoli E, Sala E, Villa N, Crosti F, Chiodo F, di Cantogno LV, Savin E, Croci G, Franchi F, Venti G, Donti E, Migliori V, Pettinari A, Bonifacio S, Centrone C, Torricelli F, Rossi S, Simi P, Granata P, Casalone R, Lenzini E, Artifoni L, Pecile V, Barlati S, Bellotti D, Caufin D, Police A, Cavani S, Piombo G, Pierluigi M, Larizza L. Dalprà L, et al. Among authors: artifoni l. Genet Med. 2005 Nov-Dec;7(9):620-5. doi: 10.1097/01.gim.0000182876.57766.2d. Genet Med. 2005. PMID: 16301863 Free article.
Amplification of the Xq28 FRAXE repeats: extreme phenotype variability?
Murgia A, Polli R, Vinanzi C, Salis M, Drigo P, Artifoni L, Zacchello F. Murgia A, et al. Among authors: artifoni l. Am J Med Genet. 1996 Aug 9;64(2):441-4. doi: 10.1002/(SICI)1096-8628(19960809)64:2<441::AID-AJMG41>3.0.CO;2-C. Am J Med Genet. 1996. PMID: 8844100
FRAXA and FRAXE: new tools for the diagnosis of mental retardation.
Murgia A, Vinanzi C, Polli R, Artifoni L, Zacchello F. Murgia A, et al. Among authors: artifoni l. Acta Genet Med Gemellol (Roma). 1996;45(1-2):295-7. doi: 10.1017/s0001566000001501. Acta Genet Med Gemellol (Roma). 1996. PMID: 8872051 No abstract available.
Electroclinical diagnosis of Angelman syndrome: a study of 7 cases.
Casara GL, Vecchi M, Boniver C, Drigo P, Baccichetti C, Artifoni L, Franzoni E, Marchiani V. Casara GL, et al. Among authors: artifoni l. Brain Dev. 1995 Jan-Feb;17(1):64-8. doi: 10.1016/0387-7604(94)00104-6. Brain Dev. 1995. PMID: 7762767
Partial duplication of 17 long arm.
Lenzini E, Leszl A, Artifoni L, Casellato R, Tenconi R, Baccichetti C. Lenzini E, et al. Among authors: artifoni l. Ann Genet. 1988;31(3):175-80. Ann Genet. 1988. PMID: 3265610
Terminal deletion of the short arm of chromosome 5.
Baccichetti C, Lenzini E, Artifoni L, Caufin D, Marangoni P. Baccichetti C, et al. Among authors: artifoni l. Clin Genet. 1988 Oct;34(4):219-23. doi: 10.1111/j.1399-0004.1988.tb02868.x. Clin Genet. 1988. PMID: 3233775
A new family with extra material on proximal 15q.
Turolla L, Baccichetti C, Artifoni L, Lenzini E, Leszl A, Tenconi R. Turolla L, et al. Among authors: artifoni l. Ann Genet. 1989;32(4):230-2. Ann Genet. 1989. PMID: 2610489
34 results