Thompson MW - Search Results

1

Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophy.

Kunkel LM, Hejtmancik JF, Caskey CT, Speer A, Monaco AP, Middlesworth W, Colletti CA, Bertelson C, Müller U, Bresnan M, Shapiro F, Tantravahi U, Speer J, Latt SA, Bartlett R, Pericak-Vance MA, Roses AD, Thompson MW, Ray PN, Worton RG, Fischbeck KH, Gallano P, Coulon M, Duros C, Boue J, Junien C, Chelly J, Hamard G, Jeanpierre M, Lambert M, Kaplan JC, Emery A, Dorkins H, McGlade S, Davies KE, Boehm C, Arveiler B, Lemaire C, Morgan GJ, Denton MJ, Amos J, Bobrow M, Benham F, Boswinkel E, Cole C, Dubowitz V, Hart K, Hodgson S, Johnson L, Walker A, Roncuzzi L, Ferlini A, Nobile C, Romeo G, Wilcox DE, Affara NA, Ferguson-Smith MA, Lindolf M, Kaariainen H, de la Chapelle A, Ionasescu V, Searby C, Ionasescu R, Bakker E, van Ommen GJ, Pearson PL, Greenberg CR, Hamerton JL, Wrogemann K, Doherty RA, Polakowska R, Hyser C, Quirk S, Thomas N, Harper JF, Darras BT, Francke U. Kunkel LM, et al. Among authors: thompson mw. Nature. 1986 Jul 3-9;322(6074):73-7. doi: 10.1038/322073a0. Nature. 1986. PMID: 3014348

2

Cloning of the breakpoint of an X;21 translocation associated with Duchenne muscular dystrophy.

Ray PN, Belfall B, Duff C, Logan C, Kean V, Thompson MW, Sylvester JE, Gorski JL, Schmickel RD, Worton RG. Ray PN, et al. Among authors: thompson mw. Nature. 1985 Dec 19-1986 Jan 1;318(6047):672-5. doi: 10.1038/318672a0. Nature. 1985. PMID: 3001530

3

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: thompson mw. Am J Hum Genet. 1990 Apr;46(4):682-95. Am J Hum Genet. 1990. PMID: 2316519 Free PMC article.

4

Paternal inheritance of translocation chromosomes in a t(X;21) patient with X linked muscular dystrophy.

Kean VM, Macleod HL, Thompson MW, Ray PN, Verellen-Dumoulin C, Worton RG. Kean VM, et al. Among authors: thompson mw. J Med Genet. 1986 Dec;23(6):491-3. doi: 10.1136/jmg.23.6.491. J Med Genet. 1986. PMID: 2879921 Free PMC article.

5

Linkage analysis of polymorphisms within the DNA fragment XJ cloned from the breakpoint of an X;21 translocation associated with X linked muscular dystrophy.

Thompson MW, Ray PN, Belfall B, Duff C, Logan C, Oss I, Worton RG. Thompson MW, et al. J Med Genet. 1986 Dec;23(6):548-55. doi: 10.1136/jmg.23.6.548. J Med Genet. 1986. PMID: 2879926 Free PMC article.

6

The problem of Duchenne muscular dystrophy.

Worton RG, Ray PN, Bodrug S, Burghes AH, Hu X, Thompson MW. Worton RG, et al. Among authors: thompson mw. 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.

7

Analysis of an X-autosome translocation responsible for X-linked muscular dystrophy.

Worton RG, Ray PN, Bodrug S, Thompson MW. Worton RG, et al. Among authors: thompson mw. Cold Spring Harb Symp Quant Biol. 1986;51 Pt 1:345-8. doi: 10.1101/sqb.1986.051.01.040. Cold Spring Harb Symp Quant Biol. 1986. PMID: 3034484 No abstract available.

8

Frame-shift deletions in patients with Duchenne and Becker muscular dystrophy.

Malhotra SB, Hart KA, Klamut HJ, Thomas NS, Bodrug SE, Burghes AH, Bobrow M, Harper PS, Thompson MW, Ray PN, et al. Malhotra SB, et al. Among authors: thompson mw. Science. 1988 Nov 4;242(4879):755-9. doi: 10.1126/science.3055295. Science. 1988. PMID: 3055295

9

Genetics of Duchenne muscular dystrophy.

Worton RG, Thompson MW. Worton RG, et al. Among authors: thompson mw. Annu Rev Genet. 1988;22:601-29. doi: 10.1146/annurev.ge.22.120188.003125. Annu Rev Genet. 1988. PMID: 3071259 Review. No abstract available.

10

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: thompson mw. 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.

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