Risultati della ricerca - Stoppa‐Lyonnet, Dominique
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A guide to cancer genetics in clinical practice di Stoppa-Lyonnet, Dominique
Pubblicazione 2013testo -
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PEL: an unbiased method for estimating age-dependent genetic disease risk from pedigree data unselected for family history di Alarcon, Flora, Bourgain, Catherine, Gauthier-Villars, Marion, Planté-Bordeneuve, Violaine, Stoppa-Lyonnet, Dominique, Bonaïti-Pellié, Catherine
Pubblicazione 2009testo -
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Non-Coding Variants in BRCA1 and BRCA2 Genes: Potential Impact on Breast and Ovarian Cancer Predisposition di Santana dos Santos, Elizabeth, Lallemand, François, Burke, Leslie, Stoppa-Lyonnet, Dominique, Brown, Melissa, Caputo, Sandrine M., Rouleau, Etienne
Pubblicazione 2018testo -
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Underexpression and abnormal localization of ATM products in ataxia telangiectasia patients bearing ATM missense mutations di Jacquemin, Virginie, Rieunier, Guillaume, Jacob, Sandrine, Bellanger, Dorine, d'Enghien, Catherine Dubois, Laugé, Anthony, Stoppa-Lyonnet, Dominique, Stern, Marc-Henri
Pubblicazione 2012testo -
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Recurrent FAN1 p.W707X Pathogenic Variant Originating Before ad 1800 Underlies High Frequency of Karyomegalic Interstitial Nephritis in South Pacific Islands di Gueguen, Lorraine, Delaval, Ronan, Blanluet, Maud, Sartelet, Hervé, Leou, Sylvie, Dubois d’Enghien, Catherine, Golmard, Lisa, Stoppa-Lyonnet, Dominique, Testevuide, Pascale, Faguer, Stanislas
Pubblicazione 2021testo -
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Risk Estimation as a Decision-Making Tool for Genetic Analysis of the Breast Cancer Susceptibility Genes di Chang-Claude, Jenny, Becher, Heiko, Caligo, Maria, Eccles, Diana, Evans, Gareth, Haites, Neva, Hodgson, Shirley, Møller, Pål, Weber, Bernhard H. F., Stoppa-Lyonnet, Dominique
Pubblicazione 1999testo -
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Impact of BRCA1 and BRCA2 variants on splicing: clues from an allelic imbalance study di Caux-Moncoutier, Virginie, Pagès-Berhouet, Sabine, Michaux, Dorothée, Asselain, Bernard, Castéra, Laurent, De Pauw, Antoine, Buecher, Bruno, Gauthier-Villars, Marion, Stoppa-Lyonnet, Dominique, Houdayer, Claude
Pubblicazione 2009testo -
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Mosaicism and prenatal diagnosis options: insights from retinoblastoma di Dehainault, Catherine, Golmard, Lisa, Millot, Gaël A, Charpin, Agathe, Laugé, Anthony, Tarabeux, Julien, Aerts, Isabelle, Cassoux, Nathalie, Stoppa-Lyonnet, Dominique, Gauthier-Villars, Marion, Houdayer, Claude
Pubblicazione 2017testo -
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Psychosocial problems in women attending French, German and Spanish genetics clinics before and after targeted or multigene testing results: an observational prospective study di Brédart, Anne, Kop, Jean-Luc, Dick, Julia, Cano, Alejandra, De Pauw, Antoine, Anota, Amélie, Brunet, Joan, Devilee, Peter, Stoppa-Lyonnet, Dominique, Schmutzler, Rita, Dolbeault, Sylvie
Pubblicazione 2019testo -
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Fine mapping of whole RB1 gene deletions in retinoblastoma patients confirms PCDH8 as a candidate gene for psychomotor delay di Castéra, Laurent, Dehainault, Catherine, Michaux, Dorothée, Lumbroso-Le Rouic, Livia, Aerts, Isabelle, Doz, Francois, Pelet, Anna, Couturier, Jérôme, Stoppa-Lyonnet, Dominique, Gauthier-Villars, Marion, Houdayer, Claude
Pubblicazione 2013testo -
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Ethical, Social and Economic Issues in Familial Breast Cancer: A Compilation of Views from the E.C. Biomed II Demonstration Project di Steel, Michael, Smyth, Elizabeth, Vasen, Hans, Eccles, Diana, Evans, Gareth, Møller, Pål, Hodgson, Shirley, Stoppa-Lyonnet, Dominique, Chang-Claude, Jenny, Caligo, Maria, Morrison, Patrick, Haites, Neva
Pubblicazione 1999testo -
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ART-DeCo: easy tool for detection and characterization of cross-contamination of DNA samples in diagnostic next-generation sequencing analysis di Fiévet, Alice, Bernard, Virginie, Tenreiro, Henrique, Dehainault, Catherine, Girard, Elodie, Deshaies, Vivien, Hupe, Philippe, Delattre, Olivier, Stern, Marc-Henri, Stoppa-Lyonnet, Dominique, Golmard, Lisa, Houdayer, Claude
Pubblicazione 2019testo