Spurr NK - Search Results

1

Plectin deficiency results in muscular dystrophy with epidermolysis bullosa.

Smith FJ, Eady RA, Leigh IM, McMillan JR, Rugg EL, Kelsell DP, Bryant SP, Spurr NK, Geddes JF, Kirtschig G, Milana G, de Bono AG, Owaribe K, Wiche G, Pulkkinen L, Uitto J, McLean WH, Lane EB. Smith FJ, et al. Among authors: spurr nk. Nat Genet. 1996 Aug;13(4):450-7. doi: 10.1038/ng0896-450. Nat Genet. 1996. PMID: 8696340

2

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

3

Genetic analysis of the BRCA1 region in a large breast/ovarian family: refinement of the minimal region containing BRCA1.

Kelsell DP, Black DM, Bishop DT, Spurr NK. Kelsell DP, et al. Among authors: spurr nk. Hum Mol Genet. 1993 Nov;2(11):1823-8. doi: 10.1093/hmg/2.11.1823. Hum Mol Genet. 1993. PMID: 8281142

4

Close mapping of the focal non-epidermolytic palmoplantar keratoderma (PPK) locus associated with oesophageal cancer (TOC).

Kelsell DP, Risk JM, Leigh IM, Stevens HP, Ellis A, Hennies HC, Reis A, Weissenbach J, Bishop DT, Spurr NK, Field JK. Kelsell DP, et al. Among authors: spurr nk. Hum Mol Genet. 1996 Jun;5(6):857-60. doi: 10.1093/hmg/5.6.857. Hum Mol Genet. 1996. PMID: 8776604

5

Gene mapping using somatic cell hybrids.

Kelsell DP, Spurr NK. Kelsell DP, et al. Among authors: spurr nk. Methods Mol Biol. 1997;68:45-52. doi: 10.1385/0-89603-482-8:45. Methods Mol Biol. 1997. PMID: 9055249 No abstract available.

6

Linkage of monilethrix to the trichocyte and epithelial keratin gene cluster on 12q11-q13.

Stevens HP, Kelsell DP, Bryant SP, Bishop DT, Dawber RP, Spurr NK, Leigh IM. Stevens HP, et al. Among authors: spurr nk. J Invest Dermatol. 1996 Apr;106(4):795-7. doi: 10.1111/1523-1747.ep12346400. J Invest Dermatol. 1996. PMID: 8618025 Free article.

7

Envoplakin, a possible candidate gene for focal NEPPK/esophageal cancer (TOC): the integration of genetic and physical maps of the TOC region on 17q25.

Risk JM, Ruhrberg C, Hennies H, Mills HS, Di Colandrea T, Evans KE, Ellis A, Watt FM, Bishop DT, Spurr NK, Stevens HP, Leigh IM, Reis A, Kelsell DP, Field JK. Risk JM, et al. Among authors: spurr nk. Genomics. 1999 Jul 15;59(2):234-42. doi: 10.1006/geno.1999.5857. Genomics. 1999. PMID: 10409435

8

An XmnI RFLP detected with a probe for the CYP2E gene locus on chromosome 10.

Kelsell DP, Wolf CR, Spurr NK. Kelsell DP, et al. Among authors: spurr nk. Nucleic Acids Res. 1990 May 25;18(10):3111. doi: 10.1093/nar/18.10.3111. Nucleic Acids Res. 1990. PMID: 1971937 Free PMC article.

9

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

10

The human complement C8G gene, a member of the lipocalin gene family: polymorphisms and mapping to chromosome 9q34.3.

Dewald G, Cichon S, Bryant SP, Hemmer S, Nöthen MM, Spurr NK. Dewald G, et al. Among authors: spurr nk. Ann Hum Genet. 1996 Jul;60(4):281-91. doi: 10.1111/j.1469-1809.1996.tb01192.x. Ann Hum Genet. 1996. PMID: 8865989

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