Worton RG - Search Results

1

Physical mapping at a potential X-linked retinitis pigmentosa locus (RP3) by pulsed-field gel electrophoresis.

Musarella MA, Anson-Cartwright CL, McDowell C, Burghes AH, Coulson SE, Worton RG, Rommens JM. Musarella MA, et al. Among authors: worton rg. Genomics. 1991 Oct;11(2):263-72. doi: 10.1016/0888-7543(91)90132-x. Genomics. 1991. PMID: 1769646

2

Linkage analysis of a large Latin-American family with X-linked retinitis pigmentosa and metallic sheen in the heterozygote carrier.

Musarella MA, Anson-Cartwright L, Burghes A, Worton RG, Lesko JG, Nussbaum RL. Musarella MA, et al. Among authors: worton rg. Genomics. 1989 May;4(4):601-5. doi: 10.1016/0888-7543(89)90285-1. Genomics. 1989. PMID: 2568332

3

Assignment of the gene for complete X-linked congenital stationary night blindness (CSNB1) to Xp11.3.

Musarella MA, Weleber RG, Murphey WH, Young RS, Anson-Cartwright L, Mets M, Kraft SP, Polemeno R, Litt M, Worton RG. Musarella MA, et al. Among authors: worton rg. Genomics. 1989 Nov;5(4):727-37. doi: 10.1016/0888-7543(89)90114-6. Genomics. 1989. PMID: 2574143

4

Mapping of four translocation breakpoints within the Duchenne muscular dystrophy gene.

Bodrug SE, Burghes AH, Ray PM, Worton RG. Bodrug SE, et al. Among authors: worton rg. Genomics. 1989 Jan;4(1):101-4. doi: 10.1016/0888-7543(89)90321-2. Genomics. 1989. PMID: 2914705

5

Linkage analysis in X-linked ocular albinism.

Schnur RE, Nussbaum RL, Anson-Cartwright L, McDowell C, Worton RG, Musarella MA. Schnur RE, et al. Among authors: worton rg. Genomics. 1991 Apr;9(4):605-13. doi: 10.1016/0888-7543(91)90353-g. Genomics. 1991. PMID: 1674724

6

Multipoint linkage analysis and heterogeneity testing in 20 X-linked retinitis pigmentosa families.

Musarella MA, Anson-Cartwright L, Leal SM, Gilbert LD, Worton RG, Fishman GA, Ott J. Musarella MA, et al. Among authors: worton rg. Genomics. 1990 Oct;8(2):286-96. doi: 10.1016/0888-7543(90)90284-2. Genomics. 1990. PMID: 1979051 Free PMC article.

7

Localization of the gene for X-linked recessive type of retinitis pigmentosa (XLRP) to Xp21 by linkage analysis.

Musarella MA, Burghes A, Anson-Cartwright L, Mahtani MM, Argonza R, Tsui LC, Worton R. Musarella MA, et al. Am J Hum Genet. 1988 Oct;43(4):484-94. Am J Hum Genet. 1988. PMID: 2902787 Free PMC article.

8

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.

9

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.

10

Molecular genetics of Duchenne and Becker muscular dystrophy.

Worton RG, Burghes AH. Worton RG, et al. Int Rev Neurobiol. 1988;29:1-76. doi: 10.1016/s0074-7742(08)60083-5. Int Rev Neurobiol. 1988. PMID: 3042661 Review. No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

116 results

Search Page

Filters