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Prophylactic surgery: oophorectomy or adnexectomy?
Delaloge S, Morice P, Chompret A, Lhommé C. Delaloge S, et al. Among authors: chompret a. J Clin Oncol. 2000 Oct 1;18(19):3454-5. doi: 10.1200/JCO.2000.18.19.3454. J Clin Oncol. 2000. PMID: 11013293 No abstract available.
Sporadic multiple primary melanoma cases: CDKN2A germline mutations with a founder effect.
Auroy S, Avril MF, Chompret A, Pham D, Goldstein AM, Bianchi-Scarrà G, Frebourg T, Joly P, Spatz A, Rubino C, Demenais F, Bressac-de Paillerets B; French Hereditary Melanoma Study Group. Auroy S, et al. Among authors: chompret a. Genes Chromosomes Cancer. 2001 Nov;32(3):195-202. doi: 10.1002/gcc.1183. Genes Chromosomes Cancer. 2001. PMID: 11579459
[Clinical and genetic study in 22 patients with basal cell nevus syndrome].
Pruvost-Balland C, Gorry P, Boutet N, Magnaldo T, Mamelle G, Margulis A, Kolb F, Duvillard P, Spatz A, Brugières L, Chompret A, Avril MF. Pruvost-Balland C, et al. Among authors: chompret a. Ann Dermatol Venereol. 2006 Feb;133(2):117-23. doi: 10.1016/s0151-9638(06)70861-4. Ann Dermatol Venereol. 2006. PMID: 16508594 Review. French.
Comprehensive analysis of CDKN2A (p16INK4A/p14ARF) and CDKN2B genes in 53 melanoma index cases considered to be at heightened risk of melanoma.
Laud K, Marian C, Avril MF, Barrois M, Chompret A, Goldstein AM, Tucker MA, Clark PA, Peters G, Chaudru V, Demenais F, Spatz A, Smith MW, Lenoir GM, Bressac-de Paillerets B; French Hereditary Melanoma Study Group. Laud K, et al. Among authors: chompret a. J Med Genet. 2006 Jan;43(1):39-47. doi: 10.1136/jmg.2005.033498. Epub 2005 Jun 3. J Med Genet. 2006. PMID: 15937071 Free PMC article.
89 results