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BRCA2 mutations in hereditary breast and ovarian cancer in France.
Serova-Sinilnikova OM, Boutrand L, Stoppa-Lyonnet D, Bressac-de-Paillerets B, Dubois V, Lasset C, Janin N, Bignon YJ, Longy M, Maugard C, Lidereau R, Leroux D, Frebourg T, Mazoyer S, Lenoir GM. Serova-Sinilnikova OM, et al. Among authors: maugard c. Am J Hum Genet. 1997 May;60(5):1236-9. Am J Hum Genet. 1997. PMID: 9150172 Free PMC article. No abstract available.
Loss of heterozygosity at 7q31 in breast cancer: results from an International Collaborative Study Group. The Breast Cancer Somatic Genetics Consortium.
Devilee P, Hermans J, Eyfjörd J, Bøorresen AL, Lidereau R, Sobol H, Borg A, Cleton-Jansen AM, Oláh E, Cohen BB, Scherneck S, Hamann U, Peterlin B, Caligo M, Bignon YJ, Maugard C. Devilee P, et al. Among authors: maugard c. Genes Chromosomes Cancer. 1997 Mar;18(3):193-9. Genes Chromosomes Cancer. 1997. PMID: 9071572
Marker segregation information in breast/ovarian cancer genetic counseling: is it still useful? Groupe Génétique et Cancer de la Fédération Nationale des Centres de Lutte Contre le Cancer.
Essioux L, Girodet C, Sinilnikova O, Pagès S, Eisinger F, de Résende S, Maugard C, Lanoë D, Longy M, Bignon YJ, Sobol H, Bonaïti-Pellié C, Stoppa-Lyonnet D. Essioux L, et al. Among authors: maugard c. Am J Med Genet. 1998 Sep 23;79(3):175-83. doi: 10.1002/(sici)1096-8628(19980923)79:3<175::aid-ajmg5>3.0.co;2-m. Am J Med Genet. 1998. PMID: 9788557
Cancer genetic clinics: why do women who already have cancer attend?
Julian-Reynier C, Eisinger F, Chabal F, Aurran Y, Bignon YJ, Noguès C, Machelard M, Maugard C, Vennin P, Sobol H. Julian-Reynier C, et al. Among authors: maugard c. Eur J Cancer. 1998 Sep;34(10):1549-53. doi: 10.1016/s0959-8049(98)00164-6. Eur J Cancer. 1998. PMID: 9893626
Low frequency of microsatellite instability in BRCA1 mutated breast tumours.
Vaurs-Barrière C, Penault-Llorca F, Laplace-Marieze V, Presneau N, Maugard CM, Fiche M, Hardouin A, Bignon YJ. Vaurs-Barrière C, et al. Among authors: maugard cm. J Med Genet. 2000 Oct;37(10):E32. doi: 10.1136/jmg.37.10.e32. J Med Genet. 2000. PMID: 11015464 Free PMC article. No abstract available.
112 results