A novel duplication polymorphism in the FANCA promoter and its association with breast and ovarian cancer

The FANCA gene is one of the genes in which mutations lead to Fanconi anaemia, a rare autosomal recessive disorder characterised by congenital abnormalities, bone marrow failure, and predisposition to malignancy. FANCA is also a potential breast and ovarian cancer susceptibility gene. A novel allele...

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Detalles Bibliográficos
Autores principales: Thompson, Ella, Dragovic, Rebecca L, Stephenson, Sally-Anne, Eccles, Diana M, Campbell, Ian G, Dobrovic, Alexander
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2005
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1112586/
https://www.ncbi.nlm.nih.gov/pubmed/15860134
http://dx.doi.org/10.1186/1471-2407-5-43

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1112586/
https://www.ncbi.nlm.nih.gov/pubmed/15860134
http://dx.doi.org/10.1186/1471-2407-5-43

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