Smith TJ - Search Results

1

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: smith tj. 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.

2

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: smith tj. Lancet. 1987 Dec 5;2(8571):1294-7. doi: 10.1016/s0140-6736(87)91192-5. Lancet. 1987. PMID: 2890901

3

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. Among authors: smith tj. 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.

4

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. Among authors: smith tj. J Muscle Res Cell Motil. 1988 Feb;9(1):1-8. doi: 10.1007/BF01682143. J Muscle Res Cell Motil. 1988. PMID: 3292577 Review.

5

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: smith tj. 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.

6

Localisation of the endpoints of deletions in the 5' region of the Duchenne gene using a sequence isolated by chromosome jumping.

Kenwrick SJ, Smith TJ, England S, Collins F, Davies KE. Kenwrick SJ, et al. Among authors: smith tj. Nucleic Acids Res. 1988 Feb 25;16(4):1305-17. doi: 10.1093/nar/16.4.1305. Nucleic Acids Res. 1988. PMID: 3347492 Free PMC article.

7

Duchenne and Becker muscular dystrophy mutations: analysis using 2.6 kb of muscle cDNA from the 5' end of the gene.

Smith TJ, Forrest SM, Cross GS, Davies KE. Smith TJ, et al. Nucleic Acids Res. 1987 Dec 10;15(23):9761-9. doi: 10.1093/nar/15.23.9761. Nucleic Acids Res. 1987. PMID: 3697082 Free PMC article.

8

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: smith tj. Genomics. 1991 May;10(1):57-67. doi: 10.1016/0888-7543(91)90484-v. Genomics. 1991. PMID: 2045110

9

Molecular analysis of Duchenne and Becker muscular dystrophies.

Love DR, Forrest SM, Smith TJ, England S, Flint T, Davies KE, Speer A. Love DR, et al. Among authors: smith tj. Br Med Bull. 1989 Jul;45(3):659-80. doi: 10.1093/oxfordjournals.bmb.a072351. Br Med Bull. 1989. PMID: 2688822 Review.

10

Isolation of a conserved sequence deleted in Duchenne muscular dystrophy patients.

Smith TJ, Wilson L, Kenwrick SJ, Forrest SM, Speer A, Coutelle C, Davies KE. Smith TJ, et al. Nucleic Acids Res. 1987 Mar 11;15(5):2167-74. doi: 10.1093/nar/15.5.2167. Nucleic Acids Res. 1987. PMID: 3562224 Free PMC article.

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