Bryant SP - 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: bryant sp. 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: bryant sp. Hum Mol Genet. 1995 Jun;4(6):1021-5. doi: 10.1093/hmg/4.6.1021. Hum Mol Genet. 1995. PMID: 7544664

3

N-terminal deletion in a desmosomal cadherin causes the autosomal dominant skin disease striate palmoplantar keratoderma.

Rickman L, Simrak D, Stevens HP, Hunt DM, King IA, Bryant SP, Eady RA, Leigh IM, Arnemann J, Magee AI, Kelsell DP, Buxton RS. Rickman L, et al. Among authors: bryant sp. Hum Mol Genet. 1999 Jun;8(6):971-6. doi: 10.1093/hmg/8.6.971. Hum Mol Genet. 1999. PMID: 10332028

4

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: bryant sp. J Invest Dermatol. 1996 Apr;106(4):795-7. doi: 10.1111/1523-1747.ep12346400. J Invest Dermatol. 1996. PMID: 8618025 Free article.

5

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: bryant sp. Ann Hum Genet. 1995 Oct;59(4):413-34. doi: 10.1111/j.1469-1809.1995.tb00760.x. Ann Hum Genet. 1995. PMID: 8579334

6

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: bryant sp. Ann Hum Genet. 1996 Jul;60(4):281-91. doi: 10.1111/j.1469-1809.1996.tb01192.x. Ann Hum Genet. 1996. PMID: 8865989

7

Mapping of the human adenosine A2a receptor gene: relationship to potential schizophrenia loci on chromosome 22q and exclusion from the CATCH 22 region.

Deckert J, Nöthen MM, Bryant SP, Schuffenhauer S, Schofield PR, Spurr NK, Propping P. Deckert J, et al. Among authors: bryant sp. Hum Genet. 1997 Mar;99(3):326-8. doi: 10.1007/s004390050366. Hum Genet. 1997. PMID: 9050917

8

European Gene Mapping Project (EUROGEM): genetic maps based on the CEPH reference families.

Spurr NK, Bryant SP, Attwood J, Nyberg K, Cox SA, Mills A, Bains R, Warne D, Cullin L, Povey S, et al. Spurr NK, et al. Among authors: bryant sp. Eur J Hum Genet. 1994;2(3):193-203. doi: 10.1159/000472364. Eur J Hum Genet. 1994. PMID: 7834280 No abstract available.

9

Integrated radiation hybrid and yeast artificial chromosome map of chromosome 9p.

Bouzyk M, Bryant SP, Evans C, Guioli S, Ford S, Schmidt K, Goodfellow PN, Povey S, Rebello M, Rousseaux S, Spurr NK. Bouzyk M, et al. Among authors: bryant sp. Eur J Hum Genet. 1997 Sep-Oct;5(5):299-307. Eur J Hum Genet. 1997. PMID: 9412787

10

Linkage of an American pedigree with palmoplantar keratoderma and malignancy (palmoplantar ectodermal dysplasia type III) to 17q24. Literature survey and proposed updated classification of the keratodermas.

Stevens HP, Kelsell DP, Bryant SP, Bishop DT, Spurr NK, Weissenbach J, Marger D, Marger RS, Leigh IM. Stevens HP, et al. Among authors: bryant sp. Arch Dermatol. 1996 Jun;132(6):640-51. Arch Dermatol. 1996. PMID: 8651714 Review.

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