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fanconi anemia complementation group g

Known as: FANCG, FANCONI ANEMIA, COMPLEMENTATION GROUP G 
Fanconi anemia caused by mutations of the FANCG gene.
National Institutes of Health

Papers overview

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Highly Cited
2013
Highly Cited
2013
Current methods for detecting mutations in Fanconi anemia (FA)-suspected patients are inefficient and often miss mutations. We… Expand
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Review
2012
Review
2012
Abstract Fanconi anaemia (FA) is a genetic disease featuring bone marrow failure, proneness to malignancies, and chromosomal… Expand
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2008
2008
Although brain development abnormalities and brain cancer predisposition have been reported in some Fanconi patients, the… Expand
2007
2007
Bladder carcinomas frequently show extensive deletions of chromosomes 9p and/or 9q, potentially including the loci of the Fanconi… Expand
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Highly Cited
2006
Highly Cited
2006
BACKGROUND & AIMS How specifically to treat pancreatic and other cancers harboring Fanconi anemia gene mutations has raised great… Expand
Highly Cited
2004
Highly Cited
2004
Patients with Fanconi anemia (FA) display a wide variety of defects including bone marrow failure and a high risk of developing… Expand
Highly Cited
2003
Highly Cited
2003
Fanconi anaemia (FA) is an autosomal recessive genetic disorder characterized by progressive bone marrow failure, multiple… Expand
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2003
2003
Fanconi anemia (FA) is a genetically heterogeneous autosomal recessive syndrome associated with chromosomal instability… Expand
Highly Cited
2002
Highly Cited
2002
Fanconi anemia (FA) is a genetic disorder that leads to aplastic anemia and birth defects and predisposes to cancer. FA cells… Expand
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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… Expand
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