FANCG gene

Known as: FANCG, FAG, X-ray repair complementing defective repair in Chinese hamster cells 9 
This gene is involved in the maintenance of genomic integrity and nuclear signal transduction. Allelic variants of the gene are involved in Fanconi… (More)
National Institutes of Health

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2012
2012
Fanconi anemia (FA) is a human rare genetic disorder characterized by congenital defects, bone marrow (BM) failure and… (More)
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Highly Cited
2008
Highly Cited
2008
Fanconi anemia (FA) is a human disorder characterized by cancer susceptibility and cellular sensitivity to DNA crosslinks and… (More)
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Highly Cited
2006
Highly Cited
2006
OBJECTIVES We have undertaken a comprehensive study of common polymorphisms in genes of DNA repair, exploring both the risk of… (More)
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Highly Cited
2006
Highly Cited
2006
Lung cancer is a leading cause of cancer mortality with an inter-individual difference in susceptibility to the disease. The… (More)
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Highly Cited
2002
Highly Cited
2002
Fanconi anemia (FA) is a heterogeneous autosomal recessive chromosomal instability syndrome associated with diverse developmental… (More)
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Highly Cited
2001
Highly Cited
2001
Fanconi anemia (FA) is a human autosomal recessive cancer susceptibility disorder characterized by cellular sensitivity to… (More)
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Highly Cited
2000
Highly Cited
2000
Fanconi anemia (FA) is a chromosomal instability syndrome associated with a strong predisposition to cancer, particularly acute… (More)
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Highly Cited
1999
Highly Cited
1999
Fanconi anemia (FA) is an autosomal recessive cancer susceptibility syndrome with at least eight complementation groups (A to H… (More)
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Highly Cited
1999
Highly Cited
1999
Fanconi anemia (FA) is a recessively inherited disease characterized at the cellular level by spontaneous chromosomal instability… (More)
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Highly Cited
1998
Highly Cited
1998
Fanconi anemia (FA) is an autosomal recessive disease with diverse clinical symptoms including developmental anomalies, bone… (More)
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