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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The Promoter of the Latency-Associated Transcripts of Herpes Simplex Virus Type 1 Contains a Functional cAMP-Response Element: Role of the Latency-Associated Transcripts and cAMP i... von Leib, David A., Nadeau, Kari C., Rundle, Scott A., Schaffer, Priscilla A.

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Lead in playground dust and on the hands of schoolchildren von Duggan, M.J., Inskip, M.J., Rundle, S.A., Moorcroft, J.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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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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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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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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Studying financial inclusion in north-east India von Bhanot, Disha, Bapat, Varadraj, Bera, Sasadhar

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RFLP for a DNA clone which maps to 19q13.2-19qter (D19S63) von BROOK, J. D, HARLEY, H. G, RUNDLE, S. A, WALSH, K. V, SHAW, D. J

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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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Lead pollution from the external redecoration of old buildings von Rundle, S.A., Duggan, M.J.

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Nowcasting Great Global Earthquake and Tsunami Sources von Rundle, John B., Luginbuhl, Molly, Khapikova, Polina, Turcotte, Donald L., Donnellan, Andrea, McKim, Grayson

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A HindIII polymorphism identified by a DNA clone which maps to chromosome 17 (D17S245) von BROOK, J. D, UPADHYAYA, M, BROADHEAD, W, RUNDLE, S. A, WALSH, K. V, HARLEY, H. G, SHAW, D. J

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The physical map of chromosome arm 19q : some new assignments, confirmations and re-assessments von BROOK, J. D, KNIGHT, S. J. L, SCHONK, D, SMEETS, H, HADDINGHAM, K, SICILIANO, M. J, PALMER, D. K, MILES, J. S, WOLF, C. R, FONATSCH, C, SHAW, D. J, ROBERTS, S. H, HARLEY, H. G, WALSH, K. V, RUNDLE, S. A, FREYNE, K, KOCH, M. C, EPSTEIN, N. D, WIERINGA, B

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