Myring J - Search Results

1

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: myring j. Am J Med Genet. 1992 Aug 1;43(6):1006-11. doi: 10.1002/ajmg.1320430618. Am J Med Genet. 1992. PMID: 1415325

2

Huntington's disease: predictive testing and the molecular genetics laboratory.

Lazarou LP, Meredith AL, Myring JM, Tyler A, Morris M, Ball DM, Harper PS. Lazarou LP, et al. Among authors: myring jm. Clin Genet. 1993 Mar;43(3):150-6. doi: 10.1111/j.1399-0004.1993.tb04441.x. Clin Genet. 1993. PMID: 8098998

3

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

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

5

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. 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.

6

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: myring j. 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.

7

Size of the unstable CTG repeat sequence in relation to phenotype and parental transmission in myotonic dystrophy.

Harley HG, Rundle SA, MacMillan JC, Myring J, Brook JD, Crow S, Reardon W, Fenton I, Shaw DJ, Harper PS. Harley HG, et al. Among authors: myring j. Am J Hum Genet. 1993 Jun;52(6):1164-74. Am J Hum Genet. 1993. PMID: 8503448 Free PMC article.

8

Presymptomatic testing in myotonic dystrophy: genetic counselling approaches.

Fokstuen S, Myring J, Evans C, Harper PS. Fokstuen S, et al. Among authors: myring j. J Med Genet. 2001 Dec;38(12):846-50. doi: 10.1136/jmg.38.12.846. J Med Genet. 2001. PMID: 11768386 Free PMC article. No abstract available.

9

Presymptomatic testing for Huntington's disease in Wales 1987-90.

Tyler A, Morris M, Lazarou L, Meredith L, Myring J, Harper P. Tyler A, et al. Among authors: myring j. Br J Psychiatry. 1992 Oct;161:481-8. doi: 10.1192/bjp.161.4.481. Br J Psychiatry. 1992. PMID: 1393334

10

Eight years' experience of direct molecular testing for myotonic dystrophy in Wales.

Fokstuen S, Myring J, Meredith L, Ravine D, Harper PS. Fokstuen S, et al. Among authors: myring j. J Med Genet. 2001 Dec;38(12):E42. doi: 10.1136/jmg.38.12.e42. J Med Genet. 2001. PMID: 11748308 Free PMC article. No abstract available.

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