Stoppa-Lyonnet D - Search Results

1

Bar code screening on combed DNA for large rearrangements of the BRCA1 and BRCA2 genes in French breast cancer families.

Gad S, Klinger M, Caux-Moncoutier V, Pages-Berhouet S, Gauthier-Villars M, Coupier I, Bensimon A, Aurias A, Stoppa-Lyonnet D. Gad S, et al. J Med Genet. 2002 Nov;39(11):817-21. doi: 10.1136/jmg.39.11.817. J Med Genet. 2002. PMID: 12414821 Free PMC article. No abstract available.

2

[Ataxia telangiectasia: what impact in clinical oncology?].

Stoppa-Lyonnet D, Aurias A. Stoppa-Lyonnet D, et al. Bull Cancer. 1992;79(7):645-50. Bull Cancer. 1992. PMID: 1467590 Review. French.

3

Unusual T cell clones in a patient with Nijmegen breakage syndrome.

Stoppa-Lyonnet D, Girault D, LeDeist F, Aurias A. Stoppa-Lyonnet D, et al. J Med Genet. 1992 Feb;29(2):136-7. doi: 10.1136/jmg.29.2.136. J Med Genet. 1992. PMID: 1613764 Free PMC article.

4

Breast cancer risk in ataxia telangiectasia (AT) heterozygotes: haplotype study in French AT families.

Janin N, Andrieu N, Ossian K, Laugé A, Croquette MF, Griscelli C, Debré M, Bressac-de-Paillerets B, Aurias A, Stoppa-Lyonnet D. Janin N, et al. Br J Cancer. 1999 Jun;80(7):1042-5. doi: 10.1038/sj.bjc.6690460. Br J Cancer. 1999. PMID: 10362113 Free PMC article.

5

No evidence for germline PTEN mutations in families with breast and brain tumours.

Laugé A, Lefebvre C, Laurent-Puig P, Caux V, Gad S, Eng C, Longy M, Stoppa-Lyonnet D. Laugé A, et al. Int J Cancer. 1999 Jun 21;84(3):216-9. doi: 10.1002/(sici)1097-0215(19990621)84:3<216::aid-ijc3>3.0.co;2-e. Int J Cancer. 1999. PMID: 10371336

6

Genetic testing for breast cancer predisposition.

Gauthier-Villars M, Gad S, Caux V, Pagès S, Blandy C, Stoppa-Lyonnet D. Gauthier-Villars M, et al. Surg Clin North Am. 1999 Oct;79(5):1171-87, xxi. doi: 10.1016/s0039-6109(05)70067-0. Surg Clin North Am. 1999. PMID: 10572557 Review.

7

[Under what conditions should we propose a prophylactic mastectomy for a woman at risk?].

Gauthier-Villars M, Blandy C, Stoppa-Lyonnet D. Gauthier-Villars M, et al. Bull Cancer. 1999 Sep;86(9):754-9. Bull Cancer. 1999. PMID: 10576812 Free article. French. No abstract available.

8

Familial invasive breast cancers: worse outcome related to BRCA1 mutations.

Stoppa-Lyonnet D, Ansquer Y, Dreyfus H, Gautier C, Gauthier-Villars M, Bourstyn E, Clough KB, Magdelénat H, Pouillart P, Vincent-Salomon A, Fourquet A, Asselain B. Stoppa-Lyonnet D, et al. J Clin Oncol. 2000 Dec 15;18(24):4053-9. doi: 10.1200/JCO.2000.18.24.4053. J Clin Oncol. 2000. PMID: 11118466

9

Color bar coding the BRCA1 gene on combed DNA: a useful strategy for detecting large gene rearrangements.

Gad S, Aurias A, Puget N, Mairal A, Schurra C, Montagna M, Pages S, Caux V, Mazoyer S, Bensimon A, Stoppa-Lyonnet D. Gad S, et al. Genes Chromosomes Cancer. 2001 May;31(1):75-84. doi: 10.1002/gcc.1120. Genes Chromosomes Cancer. 2001. PMID: 11284038

10

Identification of a large rearrangement of the BRCA1 gene using colour bar code on combed DNA in an American breast/ovarian cancer family previously studied by direct sequencing.

Gad S, Scheuner MT, Pages-Berhouet S, Caux-Moncoutier V, Bensimon A, Aurias A, Pinto M, Stoppa-Lyonnet D. Gad S, et al. J Med Genet. 2001 Jun;38(6):388-92. doi: 10.1136/jmg.38.6.388. J Med Genet. 2001. PMID: 11424920 Free PMC article. No abstract available.

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