Germline DNA copy number variation in familial and early-onset breast cancer

INTRODUCTION: Genetic factors predisposing individuals to cancer remain elusive in the majority of patients with a familial or clinical history suggestive of hereditary breast cancer. Germline DNA copy number variation (CNV) has recently been implicated in predisposition to cancers such as neuroblas...

Descripción completa

Detalles Bibliográficos
Autores principales: Krepischi, Ana CV, Achatz, Maria Isabel W, Santos, Erika MM, Costa, Silvia S, Lisboa, Bianca CG, Brentani, Helena, Santos, Tiago M, Gonçalves, Amanda, Nóbrega, Amanda F, Pearson, Peter L, Vianna-Morgante, Angela M, Carraro, Dirce M, Brentani, Ricardo R, Rosenberg, Carla
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3496142/
https://www.ncbi.nlm.nih.gov/pubmed/22314128
http://dx.doi.org/10.1186/bcr3109

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3496142/
https://www.ncbi.nlm.nih.gov/pubmed/22314128
http://dx.doi.org/10.1186/bcr3109

Ejemplares similares