Bobrow M - Search Results

1

Direct detection of dystrophin gene rearrangements by analysis of dystrophin mRNA in peripheral blood lymphocytes.

Roberts RG, Barby TF, Manners E, Bobrow M, Bentley DR. Roberts RG, et al. Among authors: bobrow m. Am J Hum Genet. 1991 Aug;49(2):298-310. Am J Hum Genet. 1991. PMID: 1867192 Free PMC article.

2

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. Among authors: bobrow m. Lancet. 1990 Dec 22-29;336(8730):1523-6. doi: 10.1016/0140-6736(90)93305-9. Lancet. 1990. PMID: 1979364

3

Detection of novel genetic markers by mismatch analysis.

Roberts RG, Montandon AJ, Bobrow M, Bentley DR. Roberts RG, et al. Among authors: bobrow m. 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

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: bobrow m. Am J Hum Genet. 1995 Aug;57(2):311-20. Am J Hum Genet. 1995. PMID: 7668256 Free PMC article.

5

Point mutation in a Becker muscular dystrophy patient.

Roberts RG, Passos-Bueno MR, Bobrow M, Vainzof M, Zatz M. Roberts RG, et al. Among authors: bobrow m. Hum Mol Genet. 1993 Jan;2(1):75-7. doi: 10.1093/hmg/2.1.75. Hum Mol Genet. 1993. PMID: 7683953 No abstract available.

6

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. Among authors: bobrow m. Hum Mutat. 1994;4(1):1-11. doi: 10.1002/humu.1380040102. Hum Mutat. 1994. PMID: 7951253 Review.

7

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: bobrow m. Lancet. 1993 Jan 30;341(8840):273-5. doi: 10.1016/0140-6736(93)92618-4. Lancet. 1993. PMID: 8093919

8

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. Among authors: bobrow m. 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.

9

Exon structure of the human dystrophin gene.

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

10

Infidelity in the structure of ectopic transcripts: a novel exon in lymphocyte dystrophin transcripts.

Roberts RG, Bentley DR, Bobrow M. Roberts RG, et al. Among authors: bobrow m. Hum Mutat. 1993;2(4):293-9. doi: 10.1002/humu.1380020409. Hum Mutat. 1993. PMID: 8401537

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