Roberts RG - Search Results

1

Single base substitutions are detected by double strand conformation analysis.

Saad FA, Halliger B, Müller CR, Roberts RG, Danieli GA. Saad FA, et al. Among authors: roberts rg. Nucleic Acids Res. 1994 Oct 11;22(20):4352-3. doi: 10.1093/nar/22.20.4352. Nucleic Acids Res. 1994. PMID: 7937168 Free PMC article.

2

Exon-intron organization of the human dystrophin gene.

Nobile C, Marchi J, Nigro V, Roberts RG, Danieli GA. Nobile C, et al. Among authors: roberts rg. Genomics. 1997 Oct 15;45(2):421-4. doi: 10.1006/geno.1997.4911. Genomics. 1997. PMID: 9344670

3

Detection of novel genetic markers by mismatch analysis.

Roberts RG, Montandon AJ, Bobrow M, Bentley DR. Roberts RG, et al. Nucleic Acids Res. 1989 Aug 11;17(15):5961-71. doi: 10.1093/nar/17.15.5961. Nucleic Acids Res. 1989. PMID: 2570401 Free PMC article.

4

A MseI polymorphism in exon 48 of the dystrophin gene.

Yau SC, Roberts RG, Bentley DR, Mathew CG, Bobrow M. Yau SC, et al. Among authors: roberts rg. Nucleic Acids Res. 1991 Oct 25;19(20):5803. doi: 10.1093/nar/19.20.5803-a. Nucleic Acids Res. 1991. PMID: 1682892 Free PMC article.

5

A MaeIII polymorphism near the dystrophin gene promoter by restriction of amplified DNA.

Roberts RG, Bobrow M, Bentley DR. Roberts RG, et al. Nucleic Acids Res. 1990 Mar 11;18(5):1315. Nucleic Acids Res. 1990. PMID: 1969623 Free PMC article.

6

Rapid carrier and prenatal diagnosis of Duchenne and Becker muscular dystrophy.

Roberts RG, Cole CG, Hart KA, Bobrow M, Bentley DR. Roberts RG, et al. Nucleic Acids Res. 1989 Jan 25;17(2):811. doi: 10.1093/nar/17.2.811. Nucleic Acids Res. 1989. PMID: 2563578 Free PMC article.

7

Deletions in the 5' region of dystrophin and resulting phenotypes.

Muntoni F, Gobbi P, Sewry C, Sherratt T, Taylor J, Sandhu SK, Abbs S, Roberts R, Hodgson SV, Bobrow M, et al. Muntoni F, et al. J Med Genet. 1994 Nov;31(11):843-7. doi: 10.1136/jmg.31.11.843. J Med Genet. 1994. PMID: 7853367 Free PMC article.

8

Searching for the 1 in 2,400,000: a review of dystrophin gene point mutations.

Roberts RG, Gardner RJ, Bobrow M. Roberts RG, et al. Hum Mutat. 1994;4(1):1-11. doi: 10.1002/humu.1380040102. Hum Mutat. 1994. PMID: 7951253 Review.

9

Protein truncation test: analysis of two novel point mutations at the carboxy-terminus of the human dystrophin gene associated with mental retardation.

Tuffery S, Lenk U, Roberts RG, Coubes C, Demaille J, Claustres M. Tuffery S, et al. Among authors: roberts rg. Hum Mutat. 1995;6(2):126-35. doi: 10.1002/humu.1380060205. Hum Mutat. 1995. PMID: 7581396

10

Exon structure of the human dystrophin gene.

Roberts RG, Coffey AJ, Bobrow M, Bentley DR. Roberts RG, et al. Genomics. 1993 May;16(2):536-8. doi: 10.1006/geno.1993.1225. Genomics. 1993. PMID: 8314593

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