Associated Papers
Clinical and molecular features associated with biallelic mutations in FANCD1/BRCA2.
Alter BP et al.
Journal of Medical Genetics, 2007
Inducibility of nuclear Rad51 foci after DNA damage distinguishes all Fanconi anemia complementation groups from D1/BRCA2.
Godthelp BC et al.
Mutation Research, 2006
X-linked inheritance of Fanconi anemia complementation group B.
Meetei AR et al.
Nature Genetics, 2004
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