Cargando…
One test to identify 50% of all Norwegian BRCA1 mutations
Autores principales: | Møller, P, Hovig, E, Lycke, K, Stacy, RAP, Dahlberg, OJ, Hagen, A, Hagen, B, Løvslett, K, Qvist, H, Heimdal, K |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2000
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3300845/ http://dx.doi.org/10.1186/bcr147 |
Ejemplares similares
-
BRCA1 1675delA and 1135insA Account for One Third of Norwegian Familial Breast-Ovarian Cancer and Are Associated with Later Disease Onset than Less Frequent Mutations
por: Borg, Åke, et al.
Publicado: (1999) -
Survival in Norwegian BRCA1 mutation carriers with breast cancer
por: Hagen, Anne Irene, et al.
Publicado: (2009) -
Ten modifiers of BRCA1 penetrance validated in a Norwegian series
por: Heramb, Cecilie, et al.
Publicado: (2015) -
Uptake of Genetic Testing and Pre-Test Levels of Mental Distress in Norwegian Families with Known BRCA1 Mutations
por: Reichelt, Jon G., et al.
Publicado: (1999) -
Cerebral blood flow and oxidative metabolism during human endotoxaemia
por: Møller, K, et al.
Publicado: (2001)