Evaluation of BRCA1 and BRCA2 mutation prevalence, risk prediction models and a multistep testing approach in French‐Canadian families with high risk of breast and ovarian cancer

BACKGROUND AND OBJECTIVE: In clinical settings with fixed resources allocated to predictive genetic testing for high‐risk cancer predisposition genes, optimal strategies for mutation screening programmes are critically important. These depend on the mutation spectrum found in the population under co...

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Detalhes bibliográficos
Main Authors: Simard, Jacques, Dumont, Martine, Moisan, Anne‐Marie, Gaborieau, Valérie, Vézina, Hélène, Durocher, Francine, Chiquette, Jocelyne, Plante, Marie, Avard, Denise, Bessette, Paul, Brousseau, Claire, Dorval, Michel, Godard, Béatrice, Houde, Louis, Joly, Yann, Lajoie, Marie‐Andrée, Leblanc, Gilles, Lépine, Jean, Lespérance, Bernard, Malouin, Hélène, Parboosingh, Jillian, Pichette, Roxane, Provencher, Louise, Rhéaume, Josée, Sinnett, Daniel, Samson, Carolle, Simard, Jean‐Claude, Tranchant, Martine, Voyer, Patricia, BRCAs, INHERIT, Easton, Douglas, Tavtigian, Sean V, Knoppers, Bartha‐Maria, Laframboise, Rachel, Bridge, Peter, Goldgar, David
Formato: Artigo
Idioma:Inglês
Publicado em: BMJ Group 2007
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Original Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2598057/
https://ncbi.nlm.nih.gov/pubmed/16905680
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2006.044388
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