Davies KE - Search Results

1

Effective strategy for prenatal prediction of Duchenne and Becker muscular dystrophy.

Forrest SM, Smith TJ, Cross GS, Read AP, Thomas NS, Mountford RC, Harper PS, Geirsson RT, Davies KE. Forrest SM, et al. Among authors: davies ke. Lancet. 1987 Dec 5;2(8571):1294-7. doi: 10.1016/s0140-6736(87)91192-5. Lancet. 1987. PMID: 2890901

2

Sequences of junction fragments in the deletion-prone region of the dystrophin gene.

Love DR, England SB, Speer A, Marsden RF, Bloomfield JF, Roche AL, Cross GS, Mountford RC, Smith TJ, Davies KE. Love DR, et al. Among authors: davies ke. Genomics. 1991 May;10(1):57-67. doi: 10.1016/0888-7543(91)90484-v. Genomics. 1991. PMID: 2045110

3

Very mild muscular dystrophy associated with the deletion of 46% of dystrophin.

England SB, Nicholson LV, Johnson MA, Forrest SM, Love DR, Zubrzycka-Gaarn EE, Bulman DE, Harris JB, Davies KE. England SB, et al. Among authors: davies ke. Nature. 1990 Jan 11;343(6254):180-2. doi: 10.1038/343180a0. Nature. 1990. PMID: 2404210

4

Preferential deletion of exons in Duchenne and Becker muscular dystrophies.

Forrest SM, Cross GS, Speer A, Gardner-Medwin D, Burn J, Davies KE. Forrest SM, et al. Among authors: davies ke. Nature. 1987 Oct 15-21;329(6140):638-40. doi: 10.1038/329638a0. Nature. 1987. PMID: 2821406

5

Mild and severe muscular dystrophy associated with deletions in Xp21 of the human X chromosome.

Davies KE, Smith TJ, Bundey S, Read AP, Flint T, Bell M, Speer A. Davies KE, et al. J Med Genet. 1988 Jan;25(1):9-13. doi: 10.1136/jmg.25.1.9. J Med Genet. 1988. PMID: 3162536 Free PMC article.

6

Patterns of exon deletions in Duchenne and Becker muscular dystrophy.

Read AP, Mountford RC, Forrest SM, Kenwrick SJ, Davies KE, Harris R. Read AP, et al. Among authors: davies ke. Hum Genet. 1988 Oct;80(2):152-6. doi: 10.1007/BF00702859. Hum Genet. 1988. PMID: 3169738

7

Molecular analysis of muscular dystrophy.

Davies KE, Kenwrick SJ, Patterson MN, Smith TJ, Forrest SM, Dorkins HR, Cross GS, England SB. Davies KE, et al. J Muscle Res Cell Motil. 1988 Feb;9(1):1-8. doi: 10.1007/BF01682143. J Muscle Res Cell Motil. 1988. PMID: 3292577 Review.

8

Molecular analysis and diagnosis of Duchenne muscular dystrophy.

Forrest SM, Smith TJ, Cross GS, Kenwrick SJ, England S, Flint T, Davies KE. Forrest SM, et al. Among authors: davies ke. J R Coll Physicians Lond. 1988 Apr;22(2):65-7. J R Coll Physicians Lond. 1988. PMID: 3294388 Free PMC article. Review. No abstract available.

9

Further studies of gene deletions that cause Duchenne and Becker muscular dystrophies.

Forrest SM, Cross GS, Flint T, Speer A, Robson KJ, Davies KE. Forrest SM, et al. Among authors: davies ke. Genomics. 1988 Feb;2(2):109-14. doi: 10.1016/0888-7543(88)90091-2. Genomics. 1988. PMID: 3410474

10

Deletions of fetal and adult muscle cDNA in Duchenne and Becker muscular dystrophy patients.

Cross GS, Speer A, Rosenthal A, Forrest SM, Smith TJ, Edwards Y, Flint T, Hill D, Davies KE. Cross GS, et al. Among authors: davies ke. EMBO J. 1987 Nov;6(11):3277-83. doi: 10.1002/j.1460-2075.1987.tb02646.x. EMBO J. 1987. PMID: 3428261 Free PMC article.

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