Roberts RG - Search Results

1

Accurate assessment of intragenic recombination frequency within the Duchenne muscular dystrophy gene.

Abbs S, Roberts RG, Mathew CG, Bentley DR, Bobrow M. Abbs S, et al. Among authors: roberts rg. Genomics. 1990 Aug;7(4):602-6. doi: 10.1016/0888-7543(90)90205-9. Genomics. 1990. PMID: 1974880

2

Development and validation of laboratory procedures for preimplantation diagnosis of Duchenne muscular dystrophy.

Holding C, Bentley D, Roberts R, Bobrow M, Mathew C. Holding C, et al. J Med Genet. 1993 Nov;30(11):903-9. doi: 10.1136/jmg.30.11.903. J Med Genet. 1993. PMID: 8301643 Free PMC article.

3

Determination of the exon structure of the distal portion of the dystrophin gene by vectorette PCR.

Roberts RG, Coffey AJ, Bobrow M, Bentley DR. Roberts RG, et al. Genomics. 1992 Aug;13(4):942-50. doi: 10.1016/0888-7543(92)90005-d. Genomics. 1992. PMID: 1505985

4

Point mutations in the dystrophin gene.

Roberts RG, Bobrow M, Bentley DR. Roberts RG, et al. Proc Natl Acad Sci U S A. 1992 Mar 15;89(6):2331-5. doi: 10.1073/pnas.89.6.2331. Proc Natl Acad Sci U S A. 1992. PMID: 1549596 Free PMC article.

5

Direct diagnosis of carriers of Duchenne and Becker muscular dystrophy by amplification of lymphocyte RNA.

Roberts RG, Bentley DR, Barby TF, Manners E, Bobrow M. Roberts RG, et al. Lancet. 1990 Dec 22-29;336(8730):1523-6. doi: 10.1016/0140-6736(90)93305-9. Lancet. 1990. PMID: 1979364

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

The identification of point mutations in Duchenne muscular dystrophy patients by using reverse-transcription PCR and the protein truncation test.

Gardner RJ, Bobrow M, Roberts RG. Gardner RJ, et al. Among authors: roberts rg. Am J Hum Genet. 1995 Aug;57(2):311-20. Am J Hum Genet. 1995. PMID: 7668256 Free PMC article.

8

Direct diagnosis of carriers of point mutations in Duchenne muscular dystrophy.

Yau SC, Roberts RG, Bobrow M, Mathew CG. Yau SC, et al. Among authors: roberts rg. Lancet. 1993 Jan 30;341(8840):273-5. doi: 10.1016/0140-6736(93)92618-4. Lancet. 1993. PMID: 8093919

9

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

10

Loss of a single amino acid from dystrophin resulting in Duchenne muscular dystrophy with retention of dystrophin protein.

Becker K, Robb SA, Hatton Z, Yau SC, Abbs S, Roberts RG. Becker K, et al. Among authors: roberts rg. Hum Mutat. 2003 Jun;21(6):651. doi: 10.1002/humu.9143. Hum Mutat. 2003. PMID: 14961551

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