Speer A - Search Results

1

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. Among authors: speer a. 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.

2

Two human cDNA molecules coding for the Duchenne muscular dystrophy (DMD) locus are highly homologous.

Rosenthal A, Speer A, Billwitz H, Cross GS, Forrest SM, Davies KE. Rosenthal A, et al. Among authors: speer a. Nucleic Acids Res. 1989 Jul 11;17(13):5391. doi: 10.1093/nar/17.13.5391. Nucleic Acids Res. 1989. PMID: 2668885 Free PMC article. No abstract available.

3

DNA amplification of a further exon of Duchenne muscular dystrophy locus increase possibilities for deletion screening.

Speer A, Rosenthal A, Billwitz H, Hanke R, Forrest SM, Love D, Davies KE, Coutelle C. Speer A, et al. Nucleic Acids Res. 1989 Jun 26;17(12):4892. doi: 10.1093/nar/17.12.4892. Nucleic Acids Res. 1989. PMID: 2783234 Free PMC article.

4

Human X chromosome markers and Duchenne muscular dystrophy.

Davies KE, Speer A, Herrmann F, Spiegler AW, McGlade S, Hofker MH, Briand P, Hanke R, Schwartz M, Steinbicker V, et al. Davies KE, et al. Among authors: speer a. Nucleic Acids Res. 1985 May 24;13(10):3419-26. doi: 10.1093/nar/13.10.3419. Nucleic Acids Res. 1985. PMID: 3859837 Free PMC article.

5

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

6

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

7

Molecular analysis of the Duchenne muscular dystrophy region using pulsed field gel electrophoresis.

Kenwrick S, Patterson M, Speer A, Fischbeck K, Davies K. Kenwrick S, et al. Among authors: speer a. Cell. 1987 Jan 30;48(2):351-7. doi: 10.1016/0092-8674(87)90438-7. Cell. 1987. PMID: 3026644

8

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: speer a. 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.

9

Nucleotide and corresponding amino acid sequence of human adult and fetal cDNA coding for portions of the Duchenne muscular dystrophy (DMD) gene.

Rosenthal A, Speer A, Billwitz H, Cross GS, Forrest SM, Davies KE. Rosenthal A, et al. Among authors: speer a. Biomed Biochim Acta. 1988;47(2):K13-5. Biomed Biochim Acta. 1988. PMID: 3178779 No abstract available.

10

Further studies of gene deletions that cause Duchenne and Becker muscular dystrophies.

Forrest SM, Cross GS, Flint T, Speer A, Robson KJ, Davies KE. Forrest SM, et al. Among authors: speer a. Genomics. 1988 Feb;2(2):109-14. doi: 10.1016/0888-7543(88)90091-2. Genomics. 1988. PMID: 3410474

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