Résultats de la recherche - Dominique Stoppa‐Lyonnet
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Risk of Serous Endometrial Carcinoma in Women With Pathogenic BRCA1/2 Variant After Risk-Reducing Salpingo-Oophorectomy par Claire Saule, Emmanuelle Mouret‐Fourme, Adrien Briaux, Véronique Becette, Roman Rouzier, Claude Houdayer, Dominique Stoppa‐Lyonnet
Publié 2017Artigo -
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Rapid detection of novelBRCA1 rearrangements in high-risk breast-ovarian cancer families using multiplex PCR of short fluorescent fragments par Federica Casilli, Zorika Christiana Di Rocco, Sophie Gad, Isabelle Tournier, Dominique Stoppa‐Lyonnet, Thierry Frébourg, Mario Tosi
Publié 2002Artigo -
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Distinct BRCA1 Rearrangements Involving the BRCA1 Pseudogene Suggest the Existence of a Recombination Hot Spot par Nadine Puget, Sophie Gad, Laure Perrin-Vidoz, Olga M. Sinilnikova, Dominique Stoppa‐Lyonnet, Gilbert Lenoir, Sylvie Mazoyer
Publié 2002Artigo -
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Non-Coding Variants in BRCA1 and BRCA2 Genes: Potential Impact on Breast and Ovarian Cancer Predisposition par Elizabeth Santana Dos Santos, François Lallemand, Leslie Burke, Dominique Stoppa‐Lyonnet, Melissa A. Brown, Sandrine M. Caputo, Étienne Rouleau
Publié 2018Revisão -
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An Alu-Mediated 6-kb Duplication in the BRCA1 Gene: A New Founder Mutation? par Nadine Puget, Olga M. Sinilnikova, Dominique Stoppa-Lyonnet, Carole Audoynaud, Sabine Pagès, Henry T. Lynch, David E. Goldgar, Gilbert Lenoir, Sylvie Mazoyer
Publié 1999Carta -
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Is the breast-conserving treatment with radiotherapy appropriate in BRCA1/2 mutation carriers? Long-term results and review of the literature par Youlia Kirova, Alexia Savignoni, Brigitte Sigal‐Zafrani, Anne de la Rochefordière, Rémy Salmon, Pascale This, Bernard Asselain, Dominique Stoppa‐Lyonnet, Alain Fourquet
Publié 2009Revisão -
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Genotype–phenotype correlations in hereditary familial retinoblastoma par Mélissa Taylor, Catherine Dehainault, Laurence Desjardins, François Doz, Christine Lévy, Xavier Sastre, Jérôme Couturier, Dominique Stoppa‐Lyonnet, Claude Houdayer, Marion Gauthier‐Villars
Publié 2006Artigo -
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Biallelic truncating FANCM mutations cause early-onset cancer but not Fanconi anemia par Massimo Bogliolo, Dominique Bluteau, James Lespinasse, Roser Pujol, Nadia Vasquez, Catherine Dubois d’Enghien, Dominique Stoppa‐Lyonnet, Thierry Leblanc, Jean Soulier, Jordi Surrallés
Publié 2017Artigo -
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Breast cancer risk in ataxia telangiectasia (AT) heterozygotes: haplotype study in French AT families par Nicolas Janin, Nadine Andrieu, Katia Ossian, Anthony Laugé, M. F. Croquette, C Griscelli, Marianne Debré, Brigitte Bressac–de Paillerets, Alain Aurias, Dominique Stoppa‐Lyonnet
Publié 1999Artigo -
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Denaturing High-Performance Liquid Chromatography Detects Reliably BRCA1 and BRCA2 Mutations par Teresa Wagner, Dominique Stoppa‐Lyonnet, E. Fleischmann, Daniela Muhr, Sabine Pagès, Therese Sandberg, Virginie Caux, Regina Moeslinger, Gudrun Langbauer, Åke Borg, Peter J. Oefner
Publié 1999Artigo -
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Incidence, Presentation, and Prognosis of Malignancies in Ataxia-Telangiectasia: A Report From the French National Registry of Primary Immune Deficiencies par Felipe Suárez, Nizar Mahlaoui, Danielle Canioni, Chantal Andriamanga, Catherine Dubois d’Enghien, Nicole Brousse, Jean‐Philippe Jaïs, Alain Fischer, Olivier Hermine, Dominique Stoppa‐Lyonnet
Publié 2014Artigo -
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Deep learning identifies morphological patterns of homologous recombination deficiency in luminal breast cancers from whole slide images par Tristan Lazard, Guillaume Bataillon, Peter Naylor, Tatiana Popova, François‐Clément Bidard, Dominique Stoppa‐Lyonnet, Marc‐Henri Stern, Étienne Decencière, Thomas Walter, Anne Vincent‐Salomon
Publié 2022Artigo -
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A deep intronic mutation in the RB1 gene leads to intronic sequence exonisation par Catherine Dehainault, Dorothée Michaux, Sabine Pagès-Berhouet, Virginie Caux‐Moncoutier, François Doz, Laurence Desjardins, Jérôme Couturier, Philippe Parent, Dominique Stoppa‐Lyonnet, Marion Gauthier‐Villars, Claude Houdayer
Publié 2007Artigo
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Biology
Genetics
Gene
Cancer
Medicine
Mutation
Oncology
Internal medicine
Breast cancer
Cancer research
Germline mutation
Allele
Computational biology
Genotype
Ovarian cancer
DNA
BRCA2 Protein
Germline
DNA repair
Single-nucleotide polymorphism
DNA damage
Exon
Phenotype
Environmental health
Genome
Gynecology
Pathology
Population
Confidence interval
Molecular biology