Stoppa-Lyonnet D - Search Results

1

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

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

Screening of inherited breast cancer with DNA markers.

Lalle P, Bignon YJ, Stoppa-Lyonnet D, Narod SA, Mazoyer S, Rio P, Courjal F, Bartholin P, Sobol H. Lalle P, et al. Lancet. 1993 May 29;341(8857):1422. Lancet. 1993. PMID: 8098837 No abstract available.

5

[Hereditary predisposition for cancer of the breast and the ovary].

Lalle P, Stoppa-Lyonnet D, Mazoyer S, Rio P, Girodet C, Hardouin A, Narod SA, Sobol H, Bignon YJ. Lalle P, et al. Bull Cancer. 1993 Oct;80(10):857-65. Bull Cancer. 1993. PMID: 8204923 French.

6

Haplotype and phenotype analysis of six recurrent BRCA1 mutations in 61 families: results of an international study.

Neuhausen SL, Mazoyer S, Friedman L, Stratton M, Offit K, Caligo A, Tomlinson G, Cannon-Albright L, Bishop T, Kelsell D, Solomon E, Weber B, Couch F, Struewing J, Tonin P, Durocher F, Narod S, Skolnick MH, Lenoir G, Serova O, Ponder B, Stoppa-Lyonnet D, Easton D, King MC, Goldgar DE. Neuhausen SL, et al. Am J Hum Genet. 1996 Feb;58(2):271-80. Am J Hum Genet. 1996. PMID: 8571953 Free PMC article.

7

Segregation of two BRCA1 mutations in a single family.

Stoppa-Lyonnet D, Fricker JP, Essioux L, Pages S, Limacher JM, Sobol H, Laurent-Puig P, Thomas G. Stoppa-Lyonnet D, et al. Am J Hum Genet. 1996 Aug;59(2):479-81. Am J Hum Genet. 1996. PMID: 8755940 Free PMC article. No abstract available.

8

BRCA1 sequence variations in 160 individuals referred to a breast/ovarian family cancer clinic. Institut Curie Breast Cancer Group.

Stoppa-Lyonnet D, Laurent-Puig P, Essioux L, Pagès S, Ithier G, Ligot L, Fourquet A, Salmon RJ, Clough KB, Pouillart P, Bonaïti-Pellié C, Thomas G. Stoppa-Lyonnet D, et al. Am J Hum Genet. 1997 May;60(5):1021-30. Am J Hum Genet. 1997. PMID: 9150149 Free PMC article.

9

Mutations at BRCA1: the medullary breast carcinoma revisited.

Eisinger F, Jacquemier J, Charpin C, Stoppa-Lyonnet D, Bressac-de Paillerets B, Peyrat JP, Longy M, Guinebretière JM, Sauvan R, Noguchi T, Birnbaum D, Sobol H. Eisinger F, et al. Cancer Res. 1998 Apr 15;58(8):1588-92. Cancer Res. 1998. PMID: 9563465

10

p53 mutations in BRCA1-associated familial breast cancer.

Schlichtholz B, Bouchind'homme B, Pagés S, Martin E, Liva S, Magdelenat H, Sastre-Garau X, Stoppa-Lyonnet D, Soussi T. Schlichtholz B, et al. Lancet. 1998 Aug 22;352(9128):622. doi: 10.1016/S0140-6736(05)79576-3. Lancet. 1998. PMID: 9746028 No abstract available.

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