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Heteroallelic monozygotic twins and triplets

1998; Wiley; Volume: 77; Issue: 2 Linguagem: Inglês

10.1002/(sici)1096-8628(19980501)77

1096-8628

Jos� Mar�a Cant�, M.Y. D�az-Gallardo, P. Barros-N��ez, Luis E. Figuera,

Genomics and Rare Diseases

American Journal of Medical GeneticsVolume 77, Issue 2 p. 166-167 Letter to the Editor Heteroallelic monozygotic twins and triplets José M. Cantú, Corresponding Author José M. Cantú División de Genética, Centro de Investigación Biomédica de Occidente, Instituto Mexicano del Seguro Social, Doctorado en Genética Humana CUCS, Universidad de Guadalajara, Guadalajara, Jalisco, MéxicoDivisión de Genética, CIBO-IMSS Ap. Postal 1-3838, Guadalajara, Jalisco, C.P. 44340, Mexico.Search for more papers by this authorM.Y. Díaz-Gallardo, M.Y. Díaz-Gallardo División de Genética, Centro de Investigación Biomédica de Occidente, Instituto Mexicano del Seguro Social, Doctorado en Genética Humana CUCS, Universidad de Guadalajara, Guadalajara, Jalisco, MéxicoSearch for more papers by this authorP. Barros-Núñez, P. Barros-Núñez División de Genética, Centro de Investigación Biomédica de Occidente, Instituto Mexicano del Seguro Social, Doctorado en Genética Humana CUCS, Universidad de Guadalajara, Guadalajara, Jalisco, MéxicoSearch for more papers by this authorL.E. Figuera, L.E. Figuera División de Genética, Centro de Investigación Biomédica de Occidente, Instituto Mexicano del Seguro Social, Doctorado en Genética Humana CUCS, Universidad de Guadalajara, Guadalajara, Jalisco, MéxicoSearch for more papers by this author José M. Cantú, Corresponding Author José M. Cantú División de Genética, Centro de Investigación Biomédica de Occidente, Instituto Mexicano del Seguro Social, Doctorado en Genética Humana CUCS, Universidad de Guadalajara, Guadalajara, Jalisco, MéxicoDivisión de Genética, CIBO-IMSS Ap. Postal 1-3838, Guadalajara, Jalisco, C.P. 44340, Mexico.Search for more papers by this authorM.Y. Díaz-Gallardo, M.Y. Díaz-Gallardo División de Genética, Centro de Investigación Biomédica de Occidente, Instituto Mexicano del Seguro Social, Doctorado en Genética Humana CUCS, Universidad de Guadalajara, Guadalajara, Jalisco, MéxicoSearch for more papers by this authorP. Barros-Núñez, P. Barros-Núñez División de Genética, Centro de Investigación Biomédica de Occidente, Instituto Mexicano del Seguro Social, Doctorado en Genética Humana CUCS, Universidad de Guadalajara, Guadalajara, Jalisco, MéxicoSearch for more papers by this authorL.E. Figuera, L.E. Figuera División de Genética, Centro de Investigación Biomédica de Occidente, Instituto Mexicano del Seguro Social, Doctorado en Genética Humana CUCS, Universidad de Guadalajara, Guadalajara, Jalisco, MéxicoSearch for more papers by this author First published: 07 January 1999 https://doi.org/10.1002/(SICI)1096-8628(19980501)77:2 3.0.CO;2-LCitations: 12AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat No abstract is available for this article. REFERENCES Cantú JM, Urrusti J, Hernández A, Del Castillo V, Macotela-Ruíz E (1973): Discordance for giant pigmented nevi in monozygotic twins. Ann Genet 6: 289–292. Google Scholar Díaz-Gallardo MY, Barros-Núñez P, Díaz CA, Hernández A, Gómez-Espinel I, Leal C, Fragoso R, Figuera L, García-Cruz D, Ramírez-Dueñas ML, Cantú JM (1995): Molecular characterization of the fragile-X syndrome in the Mexican population. Arch Med Res 26(Suppl): S77–S83. PubMedWeb of Science®Google Scholar Kruyer H, Mila M, Glover G, Carbonell P, Ballesta F, Estivil X (1994): Fragile X syndrome and the (CGG)n mutation: Two families with MZ twins. Am J Hum Genet 54: 437–442. CASPubMedWeb of Science®Google Scholar Risch NJ, Devlin B (1992): On the probability of matching DNA fingerprinting. Science 255: 717–720. 10.1126/science.1738844 CASPubMedWeb of Science®Google Scholar Zneimer S, Schneider N, Richards S (1993): In situ hybridization shows direct evidence of skewed X inactivation in one of monozygotic twin females manifesting Duchenne muscular dystrophy. Am J Med Genet 45: 601–605. 10.1002/ajmg.1320450517 CASPubMedWeb of Science®Google Scholar Citing Literature Volume77, Issue21 May 1998Pages 166-167 ReferencesRelatedInformation