Rundle SA - Search Results

1

Cataract and myotonic dystrophy: the role of molecular diagnosis.

Reardon W, MacMillan JC, Myring J, Harley HG, Rundle SA, Beck L, Harper PS, Shaw DJ. Reardon W, et al. Among authors: rundle sa. Br J Ophthalmol. 1993 Sep;77(9):579-83. doi: 10.1136/bjo.77.9.579. Br J Ophthalmol. 1993. PMID: 8218057 Free PMC article.

2

Localisation of the myotonic dystrophy locus to 19q13.2-19q13.3 and its relationship to twelve polymorphic loci on 19q.

Harley HG, Walsh KV, Rundle S, Brook JD, Sarfarazi M, Koch MC, Floyd JL, Harper PS, Shaw DJ. Harley HG, et al. Hum Genet. 1991 May;87(1):73-80. doi: 10.1007/BF01213096. Hum Genet. 1991. PMID: 2037285

3

Insertion/deletion polymorphism at D19S95 associated with the myotonic dystrophy CTG repeat.

Crow SR, Harley HG, Brook JD, Rundle SA, Shaw DJ. Crow SR, et al. Among authors: rundle sa. Hum Mol Genet. 1992 Sep;1(6):451. doi: 10.1093/hmg/1.6.451. Hum Mol Genet. 1992. PMID: 1338761 No abstract available.

4

Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy.

Harley HG, Brook JD, Rundle SA, Crow S, Reardon W, Buckler AJ, Harper PS, Housman DE, Shaw DJ. Harley HG, et al. Among authors: rundle sa. Nature. 1992 Feb 6;355(6360):545-6. doi: 10.1038/355545a0. Nature. 1992. PMID: 1346923

5

Unstable DNA sequence in myotonic dystrophy.

Harley HG, Rundle SA, Reardon W, Myring J, Crow S, Brook JD, Harper PS, Shaw DJ. Harley HG, et al. Among authors: rundle sa. Lancet. 1992 May 9;339(8802):1125-8. doi: 10.1016/0140-6736(92)90729-m. Lancet. 1992. PMID: 1349364

6

Minimal expression of myotonic dystrophy: a clinical and molecular analysis.

Reardon W, Harley HG, Brook JD, Rundle SA, Crow S, Harper PS, Shaw DJ. Reardon W, et al. Among authors: rundle sa. J Med Genet. 1992 Nov;29(11):770-3. doi: 10.1136/jmg.29.11.770. J Med Genet. 1992. PMID: 1453424 Free PMC article.

7

Identification of new DNA markers close to the myotonic dystrophy locus.

Brook JD, Harley HG, Walsh KV, Rundle SA, Siciliano MJ, Harper PS, Shaw DJ. Brook JD, et al. Among authors: rundle sa. J Med Genet. 1991 Feb;28(2):84-8. doi: 10.1136/jmg.28.2.84. J Med Genet. 1991. PMID: 1672160 Free PMC article.

8

Linkage relationships of the apolipoprotein C1 gene and a cytochrome P450 gene (CYP2A) to myotonic dystrophy.

Walsh KV, Harley HG, Brook JD, Rundle SA, Sarfarazi M, Harper PS, Shaw DJ. Walsh KV, et al. Among authors: rundle sa. Hum Genet. 1990 Aug;85(3):305-10. doi: 10.1007/BF00206751. Hum Genet. 1990. PMID: 1975560

9

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

Harley HG, Brook JD, Floyd J, Rundle SA, Crow S, Walsh KV, Thibault MC, Harper PS, Shaw DJ. Harley HG, et al. Among authors: rundle sa. Am J Hum Genet. 1991 Jul;49(1):68-75. Am J Hum Genet. 1991. PMID: 2063878 Free PMC article.

10

Genomic organization and transcriptional units at the myotonic dystrophy locus.

Shaw DJ, McCurrach M, Rundle SA, Harley HG, Crow SR, Sohn R, Thirion JP, Hamshere MG, Buckler AJ, Harper PS, et al. Shaw DJ, et al. Among authors: rundle sa. Genomics. 1993 Dec;18(3):673-9. doi: 10.1016/s0888-7543(05)80372-6. Genomics. 1993. PMID: 7905855

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