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Diagnostic issues in a family with late onset type 2 neurofibromatosis.
Evans DG, Bourn D, Wallace A, Ramsden RT, Mitchell JD, Strachan T. Evans DG, et al. J Med Genet. 1995 Jun;32(6):470-4. doi: 10.1136/jmg.32.6.470. J Med Genet. 1995. PMID: 7666400 Free PMC article.
Misleading linkage results in an NF2 presymptomatic test owing to mosaicism.
Bijlsma EK, Wallace AJ, Evans DG. Bijlsma EK, et al. J Med Genet. 1997 Nov;34(11):934-6. doi: 10.1136/jmg.34.11.934. J Med Genet. 1997. PMID: 9391890 Free PMC article.
Molecular diagnosis of spinal muscular atrophy.
Stewart H, Wallace A, McGaughran J, Mountford R, Kingston H. Stewart H, et al. Arch Dis Child. 1998 Jun;78(6):531-5. doi: 10.1136/adc.78.6.531. Arch Dis Child. 1998. PMID: 9713008 Free PMC article.
Probability of bilateral disease in people presenting with a unilateral vestibular schwannoma.
Evans DG, Lye R, Neary W, Black G, Strachan T, Wallace A, Ramsden RT. Evans DG, et al. J Neurol Neurosurg Psychiatry. 1999 Jun;66(6):764-7. doi: 10.1136/jnnp.66.6.764. J Neurol Neurosurg Psychiatry. 1999. PMID: 10329751 Free PMC article.
Molecular genetic analysis of the NF2 gene in young patients with unilateral vestibular schwannomas.
Mohyuddin A, Neary WJ, Wallace A, Wu CL, Purcell S, Reid H, Ramsden RT, Read A, Black G, Evans DG. Mohyuddin A, et al. J Med Genet. 2002 May;39(5):315-22. doi: 10.1136/jmg.39.5.315. J Med Genet. 2002. PMID: 12011146 Free PMC article.
SSCP/heteroduplex analysis.
Wallace AJ. Wallace AJ. Methods Mol Biol. 2002;187:151-63. doi: 10.1385/1-59259-273-2:151. Methods Mol Biol. 2002. PMID: 12013742 No abstract available.
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