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pubmed-article:8782494pubmed:abstractTextFanconi anemia (FA) is an autosomal recessive disease characterized by birth defects, progressive bone marrow failure and increased risk for leukemia. FA cells display chromosome breakage and increased cell killing in response to DNA crosslinking agents. At least 5 genes have been defined by cell complementation studies, but only one of these, FAC has been cloned to date. Efforts to map and isolate new FA genes by functional complementation have been hampered by the lack of immortalized FA fibroblast cell lines. Here we report the use of a novel immortalization strategy to create 4 new immortalized FA fibroblast lines, including one from the rare complementation group D.lld:pubmed
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pubmed-article:8782494pubmed:dateRevised2007-11-14lld:pubmed
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pubmed-article:8782494pubmed:articleTitleImmortalization of four new Fanconi anemia fibroblast cell lines by an improved procedure.lld:pubmed
pubmed-article:8782494pubmed:affiliationDepartment of Molecular and Medical Genetics, Oregon Health Sciences University, Portland 97201, USA.lld:pubmed
pubmed-article:8782494pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:8782494pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
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