Shaw DJ - Search Results

1

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. Among authors: shaw dj. Hum Genet. 1991 May;87(1):73-80. doi: 10.1007/BF01213096. Hum Genet. 1991. PMID: 2037285

2

Segregation of linked probes to myotonic dystrophy in a family demonstrating that 152 and APOC2 are on the same side of DM on 19q.

Johnson K, Nimmo E, Jones P, Weiss M, Savontaus ML, Anvret M, Bartlett R, Roses A, Shaw D, Harper PS, et al. Johnson K, et al. Hum Genet. 1988 Dec;80(4):379-81. doi: 10.1007/BF00273655. Hum Genet. 1988. PMID: 3198115

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: shaw dj. 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: shaw dj. 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: shaw dj. Lancet. 1992 May 9;339(8802):1125-8. doi: 10.1016/0140-6736(92)90729-m. Lancet. 1992. PMID: 1349364

6

Myotonic dystrophy: advances in molecular genetics.

Shaw DJ, Harper PS. Shaw DJ, et al. Neuromuscul Disord. 1992;2(4):241-3. doi: 10.1016/0960-8966(92)90055-b. Neuromuscul Disord. 1992. PMID: 1362366 No abstract available.

7

Molecular analysis for the myotonic dystrophy mutation in neuromuscular disorders.

MacMillan JC, Myring J, Harley HG, Reardon W, Harper PS, Shaw DJ. MacMillan JC, et al. Among authors: shaw dj. Neuromuscul Disord. 1992;2(5-6):405-11. doi: 10.1016/s0960-8966(06)80012-x. Neuromuscul Disord. 1992. PMID: 1363747

8

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: shaw dj. 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.

9

Specific molecular prenatal diagnosis for the CTG mutation in myotonic dystrophy.

Myring J, Meredith AL, Harley HG, Kohn G, Norbury G, Harper PS, Shaw DJ. Myring J, et al. Among authors: shaw dj. J Med Genet. 1992 Nov;29(11):785-8. doi: 10.1136/jmg.29.11.785. J Med Genet. 1992. PMID: 1453427 Free PMC article.

10

Anticipation in myotonic dystrophy: new light on an old problem.

Harper PS, Harley HG, Reardon W, Shaw DJ. Harper PS, et al. Among authors: shaw dj. Am J Hum Genet. 1992 Jul;51(1):10-6. Am J Hum Genet. 1992. PMID: 1609789 Free PMC article.

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