A common mutation in the FACC gene causes Fanconi anaemia in Ashkenazi Jews
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics
Link
http://www.nature.com/articles/ng0693-202.pdf
Reference30 articles.
1. Fanconi, G. Familial constitutional panmyelocytopathy, Fanconi's anemia (F.A.) I. Clinical aspects. Semin. Hematol. 4, 233–240 (1967).
2. Billardon, B. & Moustacchi, E. Comparison of the sensitivity of Fanconi's anemia and normal fibroblasts of sister-chromatic exchanges by photoaddition of mono- and bi-functional psoralens. Mutat. Res. 174, 241–246 (1986).
3. Auerbach, A.D. et al. Clastogen-induced chromosomal breakage as a marker for first trimester prenatal diagnosis of Fanconi anemia. Hum. Genet. 73, 86–8 (1986).
4. Strathdee, C.A., Duncan, A.M.V. & Buchwald, M. Evidence for at least four Fanconi anaemia genes including FACC on chromosome 9. Nature Genet. 1, 196–198 (1992).
5. Mann, W.R. et al. Fanconi anemia: evidence for linkage heterogeneity on chromosome 20q. Genomics 9, 329–337 (1991).
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