Williamson R - Search Results

1

Clinical and pathologic features of chromosome 21-linked familial Alzheimer's disease.

Mullan MJ, Giuffra L, Hardy JA, Ovenstone I, Haynes AR, James LA, Williamson R, Newton PJ, Owen MJ, Roques P, et al. Mullan MJ, et al. Among authors: williamson r. Ann N Y Acad Sci. 1991;640:177-80. doi: 10.1111/j.1749-6632.1991.tb00212.x. Ann N Y Acad Sci. 1991. PMID: 1776736 No abstract available.

2

Physical mapping around the Alzheimer disease locus on the proximal long arm of chromosome 21.

Owen MJ, James LA, Hardy JA, Williamson R, Goate AM. Owen MJ, et al. Among authors: williamson r. Am J Hum Genet. 1990 Feb;46(2):316-22. Am J Hum Genet. 1990. PMID: 2301399 Free PMC article.

3

Predisposing locus for Alzheimer's disease on chromosome 21.

Goate AM, Haynes AR, Owen MJ, Farrall M, James LA, Lai LY, Mullan MJ, Roques P, Rossor MN, Williamson R, et al. Goate AM, et al. Among authors: williamson r. Lancet. 1989 Feb 18;1(8634):352-5. doi: 10.1016/s0140-6736(89)91725-x. Lancet. 1989. PMID: 2563508

4

Evidence that a locus for familial psoriasis maps to chromosome 4q.

Matthews D, Fry L, Powles A, Weber J, McCarthy M, Fisher E, Davies K, Williamson R. Matthews D, et al. Among authors: williamson r. Nat Genet. 1996 Oct;14(2):231-3. doi: 10.1038/ng1096-231. Nat Genet. 1996. PMID: 8841203

5

The time of appearance, and quantitation, of fetal DNA in the maternal circulation.

Thomas MR, Williamson R, Craft I, Rodeck CH. Thomas MR, et al. Among authors: williamson r. Ann N Y Acad Sci. 1994 Sep 7;731:217-25. Ann N Y Acad Sci. 1994. PMID: 7944123 No abstract available.

6

Physical and genetic map of 5q31: use of fluorescence in situ hybridization data to identify errors in the CEPH database. Centre d'Etude de Polymorphisme Humain.

Westbrook CA, Le Beau MM, Neuman WL, Keinanen M, Yamaoka LH, Speer MC, Espinosa R 3rd, Nakamura Y, Williamson R, Mullan M, et al. Westbrook CA, et al. Among authors: williamson r. Cytogenet Cell Genet. 1994;67(2):86-93. doi: 10.1159/000133805. Cytogenet Cell Genet. 1994. PMID: 7913678

7

The EUROGEM map of human chromosome 22.

Riley BP, Williamson R, Vergnaud G. Riley BP, et al. Among authors: williamson r. Eur J Hum Genet. 1994;2(3):246-7. Eur J Hum Genet. 1994. PMID: 7834302 No abstract available.

8

Confirmation of genetic heterogeneity in familial psoriasis.

Matthews D, Fry L, Powles A, Weissenbach J, Williamson R. Matthews D, et al. Among authors: williamson r. J Med Genet. 1995 Jul;32(7):546-8. doi: 10.1136/jmg.32.7.546. J Med Genet. 1995. PMID: 7562968 Free PMC article.

9

A mutation in the interferon-gamma-receptor gene and susceptibility to mycobacterial infection.

Newport MJ, Huxley CM, Huston S, Hawrylowicz CM, Oostra BA, Williamson R, Levin M. Newport MJ, et al. Among authors: williamson r. N Engl J Med. 1996 Dec 26;335(26):1941-9. doi: 10.1056/NEJM199612263352602. N Engl J Med. 1996. PMID: 8960473 Free article.

10

A human regulatory subunit of type II cAMP-dependent protein kinase localized by its linkage relationship to several cloned chromosome 7q markers.

Wainwright B, Lench N, Davies K, Scambler P, Kruyer H, Williamson R, Jahnsen T, Farrall M. Wainwright B, et al. Among authors: williamson r. Cytogenet Cell Genet. 1987;45(3-4):237-9. doi: 10.1159/000132461. Cytogenet Cell Genet. 1987. PMID: 3691190 No abstract available.

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