Worton RG - Search Results

1

Dystrophin in frameshift deletion patients with Becker muscular dystrophy.

Gangopadhyay SB, Sherratt TG, Heckmatt JZ, Dubowitz V, Miller G, Shokeir M, Ray PN, Strong PN, Worton RG. Gangopadhyay SB, et al. Among authors: worton rg. Am J Hum Genet. 1992 Sep;51(3):562-70. Am J Hum Genet. 1992. PMID: 1496988 Free PMC article.

2

Duplicational mutation at the Duchenne muscular dystrophy locus: its frequency, distribution, origin, and phenotypegenotype correlation.

Hu XY, Ray PN, Murphy EG, Thompson MW, Worton RG. Hu XY, et al. Among authors: worton rg. Am J Hum Genet. 1990 Apr;46(4):682-95. Am J Hum Genet. 1990. PMID: 2316519 Free PMC article.

3

Prenatal identification of a girl with a t(X;4)(p21;q35) translocation: molecular characterisation, paternal origin, and association with muscular dystrophy.

Bodrug SE, Roberson JR, Weiss L, Ray PN, Worton RG, Van Dyke DL. Bodrug SE, et al. Among authors: worton rg. J Med Genet. 1990 Jul;27(7):426-32. doi: 10.1136/jmg.27.7.426. J Med Genet. 1990. PMID: 2395160 Free PMC article.

4

Molecular and functional analysis of the muscle-specific promoter region of the Duchenne muscular dystrophy gene.

Klamut HJ, Gangopadhyay SB, Worton RG, Ray PN. Klamut HJ, et al. Among authors: worton rg. Mol Cell Biol. 1990 Jan;10(1):193-205. doi: 10.1128/mcb.10.1.193-205.1990. Mol Cell Biol. 1990. PMID: 2403634 Free PMC article.

5

Evidence for mutation by unequal sister chromatid exchange in the Duchenne muscular dystrophy gene.

Hu XY, Burghes AH, Bulman DE, Ray PN, Worton RG. Hu XY, et al. Among authors: worton rg. Am J Hum Genet. 1989 Jun;44(6):855-63. Am J Hum Genet. 1989. PMID: 2567117 Free PMC article.

6

A grandpaternally derived de novo deletion within Xp21 initially presenting in carrier females diagnosed as Kugelberg-Welander syndrome.

Wood S, Shukin RJ, McGillivray BC, Ray PN, Worton RG. Wood S, et al. Among authors: worton rg. Am J Med Genet. 1988 Feb;29(2):419-23. doi: 10.1002/ajmg.1320290225. Am J Med Genet. 1988. PMID: 2895584

7

The problem of Duchenne muscular dystrophy.

Worton RG, Ray PN, Bodrug S, Burghes AH, Hu X, Thompson MW. Worton RG, et al. Philos Trans R Soc Lond B Biol Sci. 1988 Jun 15;319(1194):275-84. doi: 10.1098/rstb.1988.0049. Philos Trans R Soc Lond B Biol Sci. 1988. PMID: 2900521 Review.

8

Partial gene duplication in Duchenne and Becker muscular dystrophies.

Hu XY, Burghes AH, Ray PN, Thompson MW, Murphy EG, Worton RG. Hu XY, et al. Among authors: worton rg. J Med Genet. 1988 Jun;25(6):369-76. doi: 10.1136/jmg.25.6.369. J Med Genet. 1988. PMID: 3398004 Free PMC article.

9

Genomic organization of exons 22 to 25 of the dystrophin gene.

Bebchuk KG, Bulman DE, D'Souza VN, Worton RG, Ray PN. Bebchuk KG, et al. Among authors: worton rg. Hum Mol Genet. 1993 May;2(5):593-4. doi: 10.1093/hmg/2.5.593. Hum Mol Genet. 1993. PMID: 8518799 No abstract available.

10

Expression of the dystrophin isoform Dp71 in differentiating human fetal myogenic cultures.

Tennyson CN, Dally GY, Ray PN, Worton RG. Tennyson CN, et al. Among authors: worton rg. Hum Mol Genet. 1996 Oct;5(10):1559-66. doi: 10.1093/hmg/5.10.1559. Hum Mol Genet. 1996. PMID: 8894689

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