Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy von Harley, Helen G, Brook, J. David, Rundle, Shelley A, Crow, Stephen, Reardon, William, Buckler, Alan J, Harper, Peter S, Housman, David E, Shaw, Duncan J

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Size of the unstable CTG repeat sequence in relation to phenotype and parental transmission in myotonic dystrophy von HARLEY, H. G, RUNDLE, S. A, MACMILLAN, J. C, MYRING, J, BROOK, J. D, CROW, S, REARDON, W, FENTON, I, SHAW, D. J, HARPER, P. S

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Unstable DNA sequence in myotonic dystrophy von Harley, H.G, Rundle, S.A, Reardon, W, Myring, J, Crow, S, Harper, P.S, Shaw, D.J, Brook, J.D

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Anticipation in myotonic dystrophy : new light on an old problem von HARPER, P. S, HARLEY, H. G, REARDON, W, SHAW, D. J

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Genetic risks for children of women with myotonic dystrophy von KOCH, M. C, GRIMM, T, HARLEY, H. G, HARPER, P. S

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Molecular basis of myotonic dystrophy: Expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member von Brook, J.David, McCurrach, Mila E., Harley, Helen G., Buckler, Alan J., Church, Deanna, Aburatani, Hiroyuki, Hunter, Kent, Stanton, Vincent P., Thirion, Jean-Paul, Hudson, Thomas, Sohn, Robert, Zemelman, Boris, Snell, Russell G., Rundle, Shelley A., Crow, Steve, Davies, June, Shelbourne, Peggy, Buxton, Jessica, Jones, Clare, Juvonen, Vesa, Johnson, Keith, Harper, Peter S., Shaw, Duncan J., Housman, David E.

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PROMM: the expanding phenotype. A family with proximal myopathy, myotonia and deafness von Phillips, M.F, Rogers, M.T, Barnetson, R, Braun, C, Harley, H.G, Myring, J, Stevens, D, Wiles, C.M, Harper, P.S

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Genomic organization and transcriptional units at the myotonic dystrophy locus von Shaw, Duncan J., McCurrach, Mila, Rundle, Shelley A., Harley, Helen G., Crow, Stephen R., Sohn, Robert, Thirion, Jean-Paul, Hamshere, Marion G., Buckler, Alan J., Harper, Peter S., Housman, David E., Brook, J. David

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Mitochondrial DNA does not appear to influence the congenital onset type of myotonic dystrophy von Poulton, J, Harley, H G, Dasmahapatra, J, Brown, G K, Potter, C G, Sykes, B

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Detection of linkage disequilibrium between the myotonic dystrophy locus and a new polymorphic DNA marker von 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

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A study of DNA methylation in myotonic dystrophy von Shaw, D J, Chaudhary, S, Rundle, S A, Crow, S, Brook, J D, Harper, P S, Harley, H G

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Minimal expression of myotonic dystrophy: a clinical and molecular analysis von Reardon, W, Harley, H G, Brook, J D, Rundle, S A, Crow, S, Harper, P S, Shaw, D J

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Cataract and myotonic dystrophy: the role of molecular diagnosis von Reardon, W, MacMillan, J C, Myring, J, Harley, H G, Rundle, S A, Beck, L, Harper, P S, Shaw, D J

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Identification of new DNA markers close to the myotonic dystrophy locus von Brook, J D, Harley, H G, Walsh, K V, Rundle, S A, Siciliano, M J, Harper, P S, Shaw, D J

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Physical and genetic characterization of the distal segment of the myotonic dystrophy area on 19q von Jansen, Gert, de Jong, Pieter J., Amemiya, Chris, Aslanidis, Charalampos, Shaw, Duncan J., Harley, Helen G., Brook, J. David, Fenwick, Ray, Korneluk, Robert G., Tsilfidis, Catherine, Shutler, Gary, Hermens, Rosella, Wormskamp, Nicole G.M., Smeets, Hubert J.M., Wieringa, Be´

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Radiation-reduced hybrids for the myotonic dystrophy locus von Brook, J.D., Zemelman, B.V., Hadingham, K., Siciliano, M.J., Crow, S., Harley, H.G., Rundle, S.A., Buxton, J., Johnson, K., Almond, J.W., Housman, D.E., Shaw, D.J.

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Specific molecular prenatal diagnosis for the CTG mutation in myotonic dystrophy von Myring, J, Meredith, A L, Harley, H G, Kohn, G, Norbury, G, Harper, P S, Shaw, D J

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Insertion/deletion polymorphism at D19S95 associated with the myotonic dystrophy CTG repeat von Crow, S.R., Harley, H.G., Brook, J.D., Rundle, S.A., Shaw, D.J.

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A recombination event that redefines the Huntington disease region von SNELL, R. G, THOMPSON, L. M, HARPER, P. S, SHAW, D. J, TAGLE, D. A, HOLLOWAY, T. L, BARNES, G, HARLEY, H. G, SANDKUIJL, L. A, MACDONALD, M. E, COLLINS, F. S, GUSELLA, J. F

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A polymorphic DNA clone which maps to 19q13.2-19qter (D19S62) von BROOK, J. D, WALSH, K. V, HARLEY, H. G, RUNDLE, S. A, SHAW, D. J

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