Chenevix-Trench G - Search Results

1

Genetic and histopathologic evaluation of BRCA1 and BRCA2 DNA sequence variants of unknown clinical significance.

Chenevix-Trench G, Healey S, Lakhani S, Waring P, Cummings M, Brinkworth R, Deffenbaugh AM, Burbidge LA, Pruss D, Judkins T, Scholl T, Bekessy A, Marsh A, Lovelock P, Wong M, Tesoriero A, Renard H, Southey M, Hopper JL, Yannoukakos K, Brown M, Easton D, Tavtigian SV, Goldgar D, Spurdle AB; kConFab Investigators. Chenevix-Trench G, et al. Cancer Res. 2006 Feb 15;66(4):2019-27. doi: 10.1158/0008-5472.CAN-05-3546. Cancer Res. 2006. PMID: 16489001

2

NcoI RFLP of the human LHRH gene on chromosome 8p.

Healey SC, Martin NG, Chenevix-Trench G. Healey SC, et al. Nucleic Acids Res. 1991 Nov 11;19(21):6059. doi: 10.1093/nar/19.21.6059. Nucleic Acids Res. 1991. PMID: 1682898 Free PMC article.

3

MspI RFLP of FSHB on chromosome 11p.

Healey SC, Southall M, Martin NG, Chenevix-Trench G. Healey SC, et al. Nucleic Acids Res. 1991 Dec 25;19(24):6981. doi: 10.1093/nar/19.24.6981-a. Nucleic Acids Res. 1991. PMID: 1722308 Free PMC article.

4

BamHI RFLP of the inhibin beta B (INHBB) chain gene on chromosome 2.

Chenevix-Trench G, Southall M, Healey S, Stewart A, Forage R, Martin NG. Chenevix-Trench G, et al. Nucleic Acids Res. 1990 Dec 25;18(24):7469. doi: 10.1093/nar/18.24.7469-a. Nucleic Acids Res. 1990. PMID: 1979678 Free PMC article.

5

Evidence for an association between nonsyndromic cleft lip with or without cleft palate and a gene located on the long arm of chromosome 4.

Mitchell LE, Healey SC, Chenevix-Trench G. Mitchell LE, et al. Am J Hum Genet. 1995 Nov;57(5):1130-6. Am J Hum Genet. 1995. PMID: 7485164 Free PMC article.

6

Colorectal carcinomas show frequent allelic loss on the long arm of chromosome 17 with evidence for a specific target region.

Leggett B, Young J, Buttenshaw R, Thomas L, Young B, Chenevix-Trench G, Searle J, Ward M. Leggett B, et al. Br J Cancer. 1995 May;71(5):1070-3. doi: 10.1038/bjc.1995.206. Br J Cancer. 1995. PMID: 7734302 Free PMC article.

7

Distinct phenotype in maternal uniparental disomy of chromosome 14.

Healey S, Powell F, Battersby M, Chenevix-Trench G, McGill J. Healey S, et al. Am J Med Genet. 1994 Jun 1;51(2):147-9. doi: 10.1002/ajmg.1320510213. Am J Med Genet. 1994. PMID: 8092191 Review.

8

Reproductive hormone genes in mothers of spontaneous dizygotic twins: an association study.

Chenevix-Trench G, Healey S, Martin NG. Chenevix-Trench G, et al. Hum Genet. 1993 Mar;91(2):118-20. doi: 10.1007/BF00222710. Hum Genet. 1993. PMID: 8096491

9

Exclusion of APC and MCC as the gene defect in one family with familial juvenile polyposis.

Leggett BA, Thomas LR, Knight N, Healey S, Chenevix-Trench G, Searle J. Leggett BA, et al. Gastroenterology. 1993 Nov;105(5):1313-6. doi: 10.1016/0016-5085(93)90134-x. Gastroenterology. 1993. PMID: 8224634

10

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. Am J Hum Genet. 1993 Sep;53(3):760-7. Am J Hum Genet. 1993. PMID: 8352281 Free PMC article.

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