Instability versus predictability: the molecular diagnosis of myotonic dystrophy (original) (raw)
Selected References
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- Ashizawa T., Epstein H. F. Ethnic distribution of myotonic dystrophy gene. Lancet. 1991 Sep 7;338(8767):642–643. doi: 10.1016/0140-6736(91)90659-d. [DOI] [PubMed] [Google Scholar]
- Aslanidis C., Jansen G., Amemiya C., Shutler G., Mahadevan M., Tsilfidis C., Chen C., Alleman J., Wormskamp N. G., Vooijs M. Cloning of the essential myotonic dystrophy region and mapping of the putative defect. Nature. 1992 Feb 6;355(6360):548–551. doi: 10.1038/355548a0. [DOI] [PubMed] [Google Scholar]
- Brook J. D., McCurrach M. E., Harley H. G., Buckler A. J., Church D., Aburatani H., Hunter K., Stanton V. P., Thirion J. P., Hudson T. Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member. Cell. 1992 Feb 21;68(4):799–808. doi: 10.1016/0092-8674(92)90154-5. [DOI] [PubMed] [Google Scholar]
- Brunner H. G., Smeets H. J., Nillesen W., van Oost B. A., van den Biezenbos J. B., Joosten E. M., Pinckers A. J., Hamel B. C., Theeuwes A. G., Wieringa B. Myotonic dystrophy. Predictive value of normal results on clinical examination. Brain. 1991 Oct;114(Pt 5):2303–2311. doi: 10.1093/brain/114.5.2303. [DOI] [PubMed] [Google Scholar]
- Buxton J., Shelbourne P., Davies J., Jones C., Van Tongeren T., Aslanidis C., de Jong P., Jansen G., Anvret M., Riley B. Detection of an unstable fragment of DNA specific to individuals with myotonic dystrophy. Nature. 1992 Feb 6;355(6360):547–548. doi: 10.1038/355547a0. [DOI] [PubMed] [Google Scholar]
- Chakravarti A. Fragile X founder effect? Nat Genet. 1992 Jul;1(4):237–238. doi: 10.1038/ng0792-237. [DOI] [PubMed] [Google Scholar]
- Fu Y. H., Kuhl D. P., Pizzuti A., Pieretti M., Sutcliffe J. S., Richards S., Verkerk A. J., Holden J. J., Fenwick R. G., Jr, Warren S. T. Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox. Cell. 1991 Dec 20;67(6):1047–1058. doi: 10.1016/0092-8674(91)90283-5. [DOI] [PubMed] [Google Scholar]
- Fu Y. H., Pizzuti A., Fenwick R. G., Jr, King J., Rajnarayan S., Dunne P. W., Dubel J., Nasser G. A., Ashizawa T., de Jong P. An unstable triplet repeat in a gene related to myotonic muscular dystrophy. Science. 1992 Mar 6;255(5049):1256–1258. doi: 10.1126/science.1546326. [DOI] [PubMed] [Google Scholar]
- Harley H. G., Brook J. D., Floyd J., Rundle S. A., Crow S., Walsh K. V., Thibault M. C., Harper P. S., Shaw D. J. Detection of linkage disequilibrium between the myotonic dystrophy locus and a new polymorphic DNA marker. Am J Hum Genet. 1991 Jul;49(1):68–75. [PMC free article] [PubMed] [Google Scholar]
- Harley H. G., Brook J. D., Rundle S. A., Crow S., Reardon W., Buckler A. J., Harper P. S., Housman D. E., Shaw D. J. Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy. Nature. 1992 Feb 6;355(6360):545–546. doi: 10.1038/355545a0. [DOI] [PubMed] [Google Scholar]
- Harley H. G., Rundle S. A., Reardon W., Myring J., Crow S., Brook J. D., Harper P. S., Shaw D. J. Unstable DNA sequence in myotonic dystrophy. Lancet. 1992 May 9;339(8802):1125–1128. doi: 10.1016/0140-6736(92)90729-m. [DOI] [PubMed] [Google Scholar]
- Harper P. S., Harley H. G., Reardon W., Shaw D. J. Anticipation in myotonic dystrophy: new light on an old problem. Am J Hum Genet. 1992 Jul;51(1):10–16. [PMC free article] [PubMed] [Google Scholar]
- Hunter A., Tsilfidis C., Mettler G., Jacob P., Mahadevan M., Surh L., Korneluk R. The correlation of age of onset with CTG trinucleotide repeat amplification in myotonic dystrophy. J Med Genet. 1992 Nov;29(11):774–779. doi: 10.1136/jmg.29.11.774. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jansen G., Mahadevan M., Amemiya C., Wormskamp N., Segers B., Hendriks W., O'Hoy K., Baird S., Sabourin L., Lennon G. Characterization of the myotonic dystrophy region predicts multiple protein isoform-encoding mRNAs. Nat Genet. 1992 Jul;1(4):261–266. doi: 10.1038/ng0792-261. [DOI] [PubMed] [Google Scholar]
- Koch M. C., Grimm T., Harley H. G., Harper P. S. Genetic risks for children of women with myotonic dystrophy. Am J Hum Genet. 1991 Jun;48(6):1084–1091. [PMC free article] [PubMed] [Google Scholar]
- La Spada A. R., Wilson E. M., Lubahn D. B., Harding A. E., Fischbeck K. H. Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy. Nature. 1991 Jul 4;352(6330):77–79. doi: 10.1038/352077a0. [DOI] [PubMed] [Google Scholar]
- Mahadevan M., Tsilfidis C., Sabourin L., Shutler G., Amemiya C., Jansen G., Neville C., Narang M., Barceló J., O'Hoy K. Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene. Science. 1992 Mar 6;255(5049):1253–1255. doi: 10.1126/science.1546325. [DOI] [PubMed] [Google Scholar]
- Melchionda S., Cobo A., Gennarelli M., Martorell L., Fattorini C., Baiget M., Lopez de Munain A., Johnson K., Shelbourne P., Novelli G. Expansion of the myotonic dystrophy gene in Italian and Spanish patients. J Med Genet. 1992 Nov;29(11):789–790. doi: 10.1136/jmg.29.11.789. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Morton N. E., Macpherson J. N. Population genetics of the fragile-X syndrome: multiallelic model for the FMR1 locus. Proc Natl Acad Sci U S A. 1992 May 1;89(9):4215–4217. doi: 10.1073/pnas.89.9.4215. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Myring J., Meredith A. L., Harley H. G., Kohn G., Norbury G., Harper P. S., Shaw D. J. Specific molecular prenatal diagnosis for the CTG mutation in myotonic dystrophy. J Med Genet. 1992 Nov;29(11):785–788. doi: 10.1136/jmg.29.11.785. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nakahori Y., Knight S. J., Holland J., Schwartz C., Roche A., Tarleton J., Wong S., Flint T. J., Froster-Iskenius U., Bentley D. Molecular heterogeneity of the fragile X syndrome. Nucleic Acids Res. 1991 Aug 25;19(16):4355–4359. doi: 10.1093/nar/19.16.4355. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Reardon W., Harley H. G., Brook J. D., Rundle S. A., Crow S., Harper P. S., Shaw D. J. Minimal expression of myotonic dystrophy: a clinical and molecular analysis. J Med Genet. 1992 Nov;29(11):770–773. doi: 10.1136/jmg.29.11.770. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Reardon W., Hughes H. E., Green S. H., Lloyd Woolley V., Harper P. S. Anal abnormalities in childhood myotonic dystrophy--a possible source of confusion in child sexual abuse. Arch Dis Child. 1992 Apr;67(4):527–528. doi: 10.1136/adc.67.4.527. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Richards R. I., Holman K., Friend K., Kremer E., Hillen D., Staples A., Brown W. T., Goonewardena P., Tarleton J., Schwartz C. Evidence of founder chromosomes in fragile X syndrome. Nat Genet. 1992 Jul;1(4):257–260. doi: 10.1038/ng0792-257. [DOI] [PubMed] [Google Scholar]
- Sutherland G. R., Haan E. A., Kremer E., Lynch M., Pritchard M., Yu S., Richards R. I. Hereditary unstable DNA: a new explanation for some old genetic questions? Lancet. 1991 Aug 3;338(8762):289–292. doi: 10.1016/0140-6736(91)90426-p. [DOI] [PubMed] [Google Scholar]
- Tsilfidis C., MacKenzie A. E., Mettler G., Barceló J., Korneluk R. G. Correlation between CTG trinucleotide repeat length and frequency of severe congenital myotonic dystrophy. Nat Genet. 1992 Jun;1(3):192–195. doi: 10.1038/ng0692-192. [DOI] [PubMed] [Google Scholar]
- Yamagata H., Miki T., Ogihara T., Nakagawa M., Higuchi I., Osame M., Shelbourne P., Davies J., Johnson K. Expansion of unstable DNA region in Japanese myotonic dystrophy patients. Lancet. 1992 Mar 14;339(8794):692–692. doi: 10.1016/0140-6736(92)90862-w. [DOI] [PubMed] [Google Scholar]
- Yu S., Mulley J., Loesch D., Turner G., Donnelly A., Gedeon A., Hillen D., Kremer E., Lynch M., Pritchard M. Fragile-X syndrome: unique genetics of the heritable unstable element. Am J Hum Genet. 1992 May;50(5):968–980. [PMC free article] [PubMed] [Google Scholar]