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Page 1
Polymerase chain reaction (PCR) on fixed necropsy material.
Mueller RF, Taylor GR, Stewart AD, Noble JS, Quirke P, Batcup G, Ivinson A. Mueller RF, et al. J Med Genet. 1990 Jan;27(1):67-8. doi: 10.1136/jmg.27.1.67. J Med Genet. 1990. PMID: 2407848 Free PMC article. No abstract available.
Automated analysis of multiplex microsatellites.
Taylor GR, Noble JS, Mueller RF. Taylor GR, et al. Among authors: mueller rf. J Med Genet. 1994 Dec;31(12):937-43. doi: 10.1136/jmg.31.12.937. J Med Genet. 1994. PMID: 7534353 Free PMC article.
Genetic analysis of the connexin-26 M34T variant: identification of genotype M34T/M34T segregating with mild-moderate non-syndromic sensorineural hearing loss.
Houseman MJ, Ellis LA, Pagnamenta A, Di WL, Rickard S, Osborn AH, Dahl HH, Taylor GR, Bitner-Glindzicz M, Reardon W, Mueller RF, Kelsell DP. Houseman MJ, et al. Among authors: mueller rf. J Med Genet. 2001 Jan;38(1):20-5. doi: 10.1136/jmg.38.1.20. J Med Genet. 2001. PMID: 11134236 Free PMC article.
Hypervariable microsatellite for genetic diagnosis.
Taylor GR, Noble JS, Hall JL, Stewart AD, Mueller RF. Taylor GR, et al. Among authors: mueller rf. Lancet. 1989 Aug 19;2(8660):454. doi: 10.1016/s0140-6736(89)90636-3. Lancet. 1989. PMID: 2569639 No abstract available.
A common founder for the 35delG GJB2 gene mutation in connexin 26 hearing impairment.
Van Laer L, Coucke P, Mueller RF, Caethoven G, Flothmann K, Prasad SD, Chamberlin GP, Houseman M, Taylor GR, Van de Heyning CM, Fransen E, Rowland J, Cucci RA, Smith RJ, Van Camp G. Van Laer L, et al. Among authors: mueller rf. J Med Genet. 2001 Aug;38(8):515-8. doi: 10.1136/jmg.38.8.515. J Med Genet. 2001. PMID: 11483639 Free PMC article.
108 results