Fanconi anemia in Ashkenazi Jews

@article{Kutler2004FanconiAI,
  title={Fanconi anemia in Ashkenazi Jews},
  author={D. Kutler and A. Auerbach},
  journal={Familial Cancer},
  year={2004},
  volume={3},
  pages={241-248}
}
Fanconi anemia (FA) should be included among the genetic diseases that occur at high frequency in the Ashkenazi Jewish population. FA exhibits extensive genetic heterogeneity; there are currently 11 complementation groups reported, and 8 (i.e., FANCA, FANCC, FANCD1/BRCA2, FANCD2, FANCE, FANCF, FANCG, and FANCL) genes have been isolated. While patients may be from widely diverse ethnic groups, a single mutation in complementation group FA-C, c.711+4A>T (commonly known as IVS4+4A>T prior to… Expand
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  • G. Bagby
  • Medicine
  • Current opinion in hematology
  • 2003
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References

SHOWING 1-10 OF 45 REFERENCES
Mutation analysis of the Fanconi anemia gene FACC.
Positional cloning of the Fanconi anaemia group A gene
Sequence variation in the Fanconi anemia gene FAA.
Evidence for at least eight Fanconi anemia genes.
A 20-year perspective on the International Fanconi Anemia Registry (IFAR).
Novel mutations and polymorphisms in the Fanconi anemia group C gene
...
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