Forrest SM - Search Results

1

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: forrest sm. Hum Genet. 1988 Oct;80(2):152-6. doi: 10.1007/BF00702859. Hum Genet. 1988. PMID: 3169738

2

Possibilities and limitation of prenatal diagnosis and carrier determination for Duchenne and Becker muscular dystrophy using cDNA probes.

Speer A, Spiegler AW, Hanke R, Grade K, Giertler U, Schieck J, Forrest S, Davies KE, Neumann R, Bollmann R, et al. Speer A, et al. J Med Genet. 1989 Jan;26(1):1-5. doi: 10.1136/jmg.26.1.1. J Med Genet. 1989. PMID: 2918522 Free PMC article.

3

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. Nature. 1987 Oct 15-21;329(6140):638-40. doi: 10.1038/329638a0. Nature. 1987. PMID: 2821406

4

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

5

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. Among authors: forrest sm. 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.

6

Molecular analysis of human muscular dystrophies.

Davies KE, Forrest S, Smith T, Kenwrick S, Ball S, Dorkins H, Patterson M. Davies KE, et al. Muscle Nerve. 1987 Mar-Apr;10(3):191-9. doi: 10.1002/mus.880100302. Muscle Nerve. 1987. PMID: 2882417 Review.

7

Regional localisation of X chromosome short arm probes.

Paulsen K, Forrest S, Scherer G, Ropers HH, Davies K. Paulsen K, et al. Hum Genet. 1986 Oct;74(2):155-9. doi: 10.1007/BF00282079. Hum Genet. 1986. PMID: 3464558

8

Characterization of deletions in the dystrophin gene giving mild phenotypes.

Love DR, Flint TJ, Marsden RF, Bloomfield JF, Daniels RJ, Forrest SM, Gabrielli O, Giorgi P, Novelli G, Davies KE. Love DR, et al. Among authors: forrest sm. Am J Med Genet. 1990 Sep;37(1):136-42. doi: 10.1002/ajmg.1320370132. Am J Med Genet. 1990. PMID: 2240031

9

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: forrest sm. Nature. 1990 Jan 11;343(6254):180-2. doi: 10.1038/343180a0. Nature. 1990. PMID: 2404210

10

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: forrest sm. Br Med Bull. 1989 Jul;45(3):659-80. doi: 10.1093/oxfordjournals.bmb.a072351. Br Med Bull. 1989. PMID: 2688822 Review.

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