Harper PS - Search Results

1

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: harper ps. Nature. 1992 Feb 6;355(6360):545-6. doi: 10.1038/355545a0. Nature. 1992. PMID: 1346923

2

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

3

Myotonic dystrophy: advances in molecular genetics.

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

4

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: harper ps. Neuromuscul Disord. 1992;2(5-6):405-11. doi: 10.1016/s0960-8966(06)80012-x. Neuromuscul Disord. 1992. PMID: 1363747

5

Advances in myotonic dystrophy: a clinical and genetic perspective.

Reardon W, Harper PS. Reardon W, et al. Among authors: harper ps. Curr Opin Neurol Neurosurg. 1992 Oct;5(5):605-9. Curr Opin Neurol Neurosurg. 1992. PMID: 1392133 Review.

6

Five years experience of predictive testing for myotonic dystrophy using linked DNA markers.

Reardon W, Floyd JL, Myring J, Lazarou LP, Meredith AL, Harper PS. Reardon W, et al. Among authors: harper ps. Am J Med Genet. 1992 Aug 1;43(6):1006-11. doi: 10.1002/ajmg.1320430618. Am J Med Genet. 1992. PMID: 1415325

7

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: harper ps. 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.

8

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: harper ps. 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.

9

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

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

10

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: harper ps. 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.

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