Myring J - Search Results

1

Randomized trial of a specialist genetic assessment service for familial breast cancer.

Brain K, Gray J, Norman P, France E, Anglim C, Barton G, Parsons E, Clarke A, Sweetland H, Tischkowitz M, Myring J, Stansfield K, Webster D, Gower-Thomas K, Daoud R, Gateley C, Monypenny I, Singhal H, Branston L, Sampson J, Roberts E, Newcombe R, Cohen D, Rogers C, Mansel R, Harper P. Brain K, et al. Among authors: myring j. J Natl Cancer Inst. 2000 Aug 16;92(16):1345-51. doi: 10.1093/jnci/92.16.1345. J Natl Cancer Inst. 2000. PMID: 10944557 Clinical Trial.

2

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

3

BRCA1 and BRCA2 in breast cancer families from Wales: moderate mutation frequency and two recurrent mutations in BRCA1.

Lancaster JM, Carney ME, Gray J, Myring J, Gumbs C, Sampson J, Wheeler D, France E, Wiseman R, Harper P, Futreal PA. Lancaster JM, et al. Among authors: myring j. Br J Cancer. 1998 Dec;78(11):1417-20. doi: 10.1038/bjc.1998.701. Br J Cancer. 1998. PMID: 9836472 Free PMC article.

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

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

6

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.

7

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.

8

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

9

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

10

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.

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