Spurr N - Search Results

1

Haplotype analysis of two recurrent CDKN2A mutations in 10 melanoma families: evidence for common founders and independent mutations.

Pollock PM, Spurr N, Bishop T, Newton-Bishop J, Gruis N, van der Velden PA, Goldstein AM, Tucker MA, Foulkes WD, Barnhill R, Haber D, Fountain J, Hayward NK. Pollock PM, et al. Among authors: spurr n. Hum Mutat. 1998;11(6):424-31. doi: 10.1002/(SICI)1098-1004(1998)11:6<424::AID-HUMU2>3.0.CO;2-2. Hum Mutat. 1998. PMID: 9603434

2

Germline mutations of the CDKN2 gene in UK melanoma families.

Harland M, Meloni R, Gruis N, Pinney E, Brookes S, Spurr NK, Frischauf AM, Bataille V, Peters G, Cuzick J, Selby P, Bishop DT, Bishop JN. Harland M, et al. Among authors: spurr nk. Hum Mol Genet. 1997 Nov;6(12):2061-7. doi: 10.1093/hmg/6.12.2061. Hum Mol Genet. 1997. PMID: 9328469

3

CYP2D6 genotyping and the association with lung cancer susceptibility.

Wolf CR, Smith CA, Bishop T, Forman D, Gough AC, Spurr NK. Wolf CR, et al. Among authors: spurr nk. Pharmacogenetics. 1994 Apr;4(2):104-6. doi: 10.1097/00008571-199404000-00008. Pharmacogenetics. 1994. PMID: 8081411 No abstract available.

4

Genetic heterogeneity in familial malignant melanoma.

MacGeoch C, Bishop JA, Bataille V, Bishop DT, Frischauf AM, Meloni R, Cuzick J, Pinney E, Spurr NK. MacGeoch C, et al. Among authors: spurr nk. Hum Mol Genet. 1994 Dec;3(12):2195-200. doi: 10.1093/hmg/3.12.2195. Hum Mol Genet. 1994. PMID: 7881419

5

Linkage analysis of early-onset breast and ovarian cancer families, with markers on the long arm of chromosome 17.

Spurr NK, Kelsell DP, Black DM, Murday VA, Turner G, Crockford GP, Solomon E, Cartwright RA, Bishop DT. Spurr NK, et al. Am J Hum Genet. 1993 Apr;52(4):777-85. Am J Hum Genet. 1993. PMID: 8460643 Free PMC article.

6

Genetic linkage studies in non-epidermolytic palmoplantar keratoderma: evidence for heterogeneity.

Kelsell DP, Stevens HP, Ratnavel R, Bryant SP, Bishop DT, Leigh IM, Spurr NK. Kelsell DP, et al. Among authors: spurr nk. Hum Mol Genet. 1995 Jun;4(6):1021-5. doi: 10.1093/hmg/4.6.1021. Hum Mol Genet. 1995. PMID: 7544664

7

Overexpression of the oncoprotein p53 in primary hepatic tumors of childhood does not correlate with gene mutations.

Kennedy SM, Macgeogh C, Jaffe R, Spurr NK. Kennedy SM, et al. Among authors: spurr nk. Hum Pathol. 1994 May;25(5):438-42. doi: 10.1016/0046-8177(94)90114-7. Hum Pathol. 1994. PMID: 8200636

8

Development of a panel of monochromosomal somatic cell hybrids for rapid gene mapping.

Kelsell DP, Rooke L, Warne D, Bouzyk M, Cullin L, Cox S, West L, Povey S, Spurr NK. Kelsell DP, et al. Among authors: spurr nk. Ann Hum Genet. 1995 Apr;59(2):233-41. doi: 10.1111/j.1469-1809.1995.tb00743.x. Ann Hum Genet. 1995. PMID: 7625768

9

Standards for reporting alleles at highly polymorphic loci: a proposal.

Spurr NK. Spurr NK. Hum Mol Genet. 1992 Jun;1(3):211-2. doi: 10.1093/hmg/1.3.211. Hum Mol Genet. 1992. PMID: 1303183 No abstract available.

10

Integrated genetic map of human chromosome 2.

Cox S, Bryant SP, Collins A, Weissenbach J, Donis-Keller H, Koeleman BP, Steinkasserer A, Spurr NK. Cox S, et al. Among authors: spurr nk. Ann Hum Genet. 1995 Oct;59(4):413-34. doi: 10.1111/j.1469-1809.1995.tb00760.x. Ann Hum Genet. 1995. PMID: 8579334

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