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A clinical study of type 2 neurofibromatosis.
Evans DG, Huson SM, Donnai D, Neary W, Blair V, Newton V, Harris R. Evans DG, et al. Q J Med. 1992 Aug;84(304):603-18. Q J Med. 1992. PMID: 1484939
The specialty of clinical genetics: European Society of Human Genetics survey.
Harris R, Rhind JA. Harris R, et al. J Med Genet. 1993 Feb;30(2):147-52. doi: 10.1136/jmg.30.2.147. J Med Genet. 1993. PMID: 8445620 Free PMC article. No abstract available.
A disease-associated germline deletion maps the type 2 neurofibromatosis (NF2) gene between the Ewing sarcoma region and the leukaemia inhibitory factor locus.
Watson CJ, Gaunt L, Evans G, Patel K, Harris R, Strachan T. Watson CJ, et al. Hum Mol Genet. 1993 Jun;2(6):701-4. doi: 10.1093/hmg/2.6.701. Hum Mol Genet. 1993. PMID: 8102569
Genetic factors in myasthenia gravis: a family study.
Kerzin-Storrar L, Metcalfe RA, Dyer PA, Kowalska G, Ferguson I, Harris R. Kerzin-Storrar L, et al. Neurology. 1988 Jan;38(1):38-42. doi: 10.1212/wnl.38.1.38. Neurology. 1988. PMID: 3336461
Molecular genetics in the National Health Service in Britain.
Harris R, Elles R, Craufurd D, Dodge A, Ivinson A, Hodgkinson K, Mountford R, Schwartz M, Strachan T, Read A. Harris R, et al. J Med Genet. 1989 Apr;26(4):219-25. doi: 10.1136/jmg.26.4.219. J Med Genet. 1989. PMID: 2523972 Free PMC article.
Localization of a gene for Waardenburg syndrome type I.
Read AP, Foy C, Newton V, Harris R. Read AP, et al. Ann N Y Acad Sci. 1991;630:143-51. doi: 10.1111/j.1749-6632.1991.tb19583.x. Ann N Y Acad Sci. 1991. PMID: 1952585 No abstract available.
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