Identification of Alu-mediated deletions
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Orna Levran; Norman A. Doggett; Arleen D. Auerbach
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Article
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1998
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John Wiley and Sons
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English
β 501 KB
Fanconi anemia (FA) is an autosomal recessive syndrome associated with hypersensitivity to DNA cross-linking agents and predisposition to neoplasia. Eight complementation groups (AH) have been described, but the only FA genes cloned so far are FAC and FAA. We have recently identified 40 different ge