Wicking C - Search Results

1

Fine deletion mapping on the long arm of chromosome 9 in sporadic and familial basal cell carcinomas.

Shanley SM, Dawkins H, Wainwright BJ, Wicking C, Heenan P, Eldon M, Searle J, Chenevix-Trench G. Shanley SM, et al. Among authors: wicking c. Hum Mol Genet. 1995 Jan;4(1):129-33. doi: 10.1093/hmg/4.1.129. Hum Mol Genet. 1995. PMID: 7711724

2

Fine genetic mapping of the gene for nevoid basal cell carcinoma syndrome.

Wicking C, Berkman J, Wainwright B, Chenevix-Trench G. Wicking C, et al. Genomics. 1994 Aug;22(3):505-11. doi: 10.1006/geno.1994.1423. Genomics. 1994. PMID: 8001963

3

Nevoid basal cell carcinoma syndrome: review of 118 affected individuals.

Shanley S, Ratcliffe J, Hockey A, Haan E, Oley C, Ravine D, Martin N, Wicking C, Chenevix-Trench G. Shanley S, et al. Among authors: wicking c. Am J Med Genet. 1994 Apr 15;50(3):282-90. doi: 10.1002/ajmg.1320500312. Am J Med Genet. 1994. PMID: 8042673 Review.

4

Simple repeat polymorphism at the D9S151 locus.

Berkman J, Armour JA, Chenevix-Trench G, Wicking C, Wainwright B. Berkman J, et al. Among authors: wicking c. Hum Mol Genet. 1994 Jan;3(1):211. doi: 10.1093/hmg/3.1.211. Hum Mol Genet. 1994. PMID: 8162036 No abstract available.

5

Further localization of the gene for nevoid basal cell carcinoma syndrome (NBCCS) in 15 Australasian families: linkage and loss of heterozygosity.

Chenevix-Trench G, Wicking C, Berkman J, Sharpe H, Hockey A, Haan E, Oley C, Ravine D, Turner A, Goldgar D, et al. Chenevix-Trench G, et al. Among authors: wicking c. Am J Hum Genet. 1993 Sep;53(3):760-7. Am J Hum Genet. 1993. PMID: 8352281 Free PMC article.

6

Mutations of the human homolog of Drosophila patched in the nevoid basal cell carcinoma syndrome.

Hahn H, Wicking C, Zaphiropoulous PG, Gailani MR, Shanley S, Chidambaram A, Vorechovsky I, Holmberg E, Unden AB, Gillies S, Negus K, Smyth I, Pressman C, Leffell DJ, Gerrard B, Goldstein AM, Dean M, Toftgard R, Chenevix-Trench G, Wainwright B, Bale AE. Hahn H, et al. Among authors: wicking c. Cell. 1996 Jun 14;85(6):841-51. doi: 10.1016/s0092-8674(00)81268-4. Cell. 1996. PMID: 8681379 Free article.

7

Most germ-line mutations in the nevoid basal cell carcinoma syndrome lead to a premature termination of the PATCHED protein, and no genotype-phenotype correlations are evident.

Wicking C, Shanley S, Smyth I, Gillies S, Negus K, Graham S, Suthers G, Haites N, Edwards M, Wainwright B, Chenevix-Trench G. Wicking C, et al. Am J Hum Genet. 1997 Jan;60(1):21-6. Am J Hum Genet. 1997. PMID: 8981943 Free PMC article.

8

De novo mutations of the Patched gene in nevoid basal cell carcinoma syndrome help to define the clinical phenotype.

Wicking C, Gillies S, Smyth I, Shanley S, Fowles L, Ratcliffe J, Wainwright B, Chenevix-Trench G. Wicking C, et al. Am J Med Genet. 1997 Dec 19;73(3):304-7. Am J Med Genet. 1997. PMID: 9415689

9

The effects of splice site mutations in patients with naevoid basal cell carcinoma syndrome.

Smyth I, Wicking C, Wainwright B, Chenevix-Trench G. Smyth I, et al. Among authors: wicking c. Hum Genet. 1998 May;102(5):598-601. doi: 10.1007/s004390050747. Hum Genet. 1998. PMID: 9654212

10

Isolation and characterization of human patched 2 (PTCH2), a putative tumour suppressor gene inbasal cell carcinoma and medulloblastoma on chromosome 1p32.

Smyth I, Narang MA, Evans T, Heimann C, Nakamura Y, Chenevix-Trench G, Pietsch T, Wicking C, Wainwright BJ. Smyth I, et al. Among authors: wicking c. Hum Mol Genet. 1999 Feb;8(2):291-7. doi: 10.1093/hmg/8.2.291. Hum Mol Genet. 1999. PMID: 9931336

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