Localisation of the Becker muscular dystrophy gene on the short arm of the X chromosome by linkage to cloned DNA sequences (original) (raw)
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References
- Becker PE, Kiener F (1955) Eine neue X-chromosomale Muskeldystrophie. Arch Pychiat Nervenkr 193:427–448
Google Scholar - Blyth H, Carter CO, Dubowitz V, Emery AEH, Gavin J, Johnston HA, McKusick VA, Race RR, Sanger R, Tippett P (1965) Duchenne's muscular dystrophy and the Xg blood groups: a search for linkage. J Med Genet 2:157–160
Google Scholar - Canki N, Dutrillaux B, Tivadar I (1979) Dystrophie musculaire de Duchenne chez une petite fille porteuse d'une translocation t(X;3)(p21;q13) de novo. Ann Genet (Paris) 22:35–39
Google Scholar - Davies KE, Pearson PL, Harper PS, Murray JM, O'Brien T, Sarfarazi M, Williamson R (1983) Linkage analysis of two cloned DNA sequences flanking the Duchenne muscular dystrophy locus on the short arm of the human X chromosome. Nucl Acids Res 11:2303–2312
Google Scholar - Emery AEH (1976) Methodology in medical genetics. An introduction to statistical methods. Edinburgh London, Churchill Livingstone
Google Scholar - Emery AEH, Skinner R (1976) Clinical studies in benign (Beckertype) X-linked muscular dystrophy. Clin Genet 10:189–201
Google Scholar - Emery AEH, Smith CAB, Sanger R (1969) The linkage relations of the loci for benign (Becker type) X-borne muscular dystrophy, colour blindness and the Xg blood groups. Ann Hum Genet 32:261–269
Google Scholar - Greenstein RM, Reardon MP, Chan TS, Middleton AB, Mulivor RA, Greene AE, Coriell LL (1980) An (X;11) translocation in a girl with Duchenne muscular dystrophy. Cytogenet Cell Genet 27: 268
Google Scholar - Jacobs PA, Hunt PA, Mayer M, Bart RD (1981) Duchenne muscular dystrophy (DMD) in a female with an X/autosome translocation: further evidence that the DMD locus is at Xp 21. Am J Hum Genet 33:513–518
Google Scholar - Kingston HM, Thomas NST, Pearson PL, Sarfarazi M, Harper PS (1983) Genetic linkage between Becker muscular dystrophy and a polymorphic DNA sequence on the short arm of the X chromosome. J Med Genet 20:255–258
Google Scholar - Kunkel LM, Smith KD, Boyer SH, Borgaonkar DS, Watchel SS, Miller OJ, Breg WR, Jones HW Jr, Rary JM (1977) Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants. Proc Natl Acad Sci USA 74:1245–1249
Google Scholar - Lange K, Elston RC (1975) Extensions to pedigree analysis. I —likelihood calculations for simple and complex pedigrees. Hum Hered 25:95–105
Google Scholar - Laurie DA, Palmer RW, Hulten MA (1982) Chiasma derived genetic lengths and recombination fractions: chromosomes 2 and 9. Ann Hum Genet 46:233–244
Google Scholar - Lindenbaum RH, Clarke G, Patel M, Moncrieff M, Hughes JT (1979) Muscular dystrophy in an X: 1 translocation female suggests that Duchenne locus is on X chromosome short arm. J Med Genet 16:389–392
Google Scholar - Murray JM, Davies KE, Harper PS, Meredith L, Mueller CR, Williamson R (1982) Linkage relationship of a cloned DNA sequence on the short arm of the X chromosome to Duchenne muscular dystrophy. Nature 300:69–71
Google Scholar - Ott J (1974) Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies. Am J Hum Genet 26:588–597
Google Scholar - Page D, De Martinville B, Barker D, Wyman A, White R, Francke U, Botstein D (1982) Single-copy sequence hybridizes to polymorphic and homologous loci on human X and Y chromosomes. Proc Natl Acad Sci USA 79:5352–5356
Google Scholar - Sarfarazi M, Harper PS, Kingston HM, Murray JM, O'Brien T, Davies KE, Williamson R, Tippett P, Sanger R (1983) Genetic linkage relationships between the Xg blood group system and two X chromosome DNA polymorphisms in families with Duchenne and Becker muscular dystrophy. Hum Genet 65: 169–171
Google Scholar - Shaw RF, Dreifuss FE (1969) Mild and severe forms of X-linked muscular dystrophy. Arch Neurol 20:451–460
Google Scholar - Skinner R, Smith C Emery AEH (1974) Linkage between the loci for benign (Beckert-type) X-borne muscular dystrophy and deutan colour blindness. J Med Genet 11:317–320
Google Scholar - Southern EM (1975) Detection of specific sequences among DNA fragments separated by gel electrophoresis. J Mol Biol 98:503–417
Google Scholar - Spence MA, Sparkes RS, Heckenlively JR, Pearliman JT Zedalis D, Sparkes M, Crist M, Tideman S (1977) Probable genetic linkage between autosomal dominant retinitis pigmentosa (RP) and amylase (AMY2): Evidence of an RP locus on chromosome 1. Am J Hum Genet 29:397–404. Erratum, 592
Google Scholar - Zatz M, Itskan SB, Sanger R, Frota-Pessoa O, Saldanha PH (1974) New linkage data for the X-linked types of muscular dystrophy and G6PD variants, colour blindness, and Xg blood groups. J Med Genet 11:321–327
Google Scholar - Zatz M, Vianna-Morgante AM, Campos P, Diamant AJ (1981) Translocation (X;6) in a female with Duchenne muscular dystrophy: implications for the localisation of the DMD locus. J Med Genet 18:442–447
Google Scholar