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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

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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
2011
Review
2011
  • J. Soulier
  • Hematology. American Society of Hematology…
  • 2011
  • Corpus ID: 19038969
Fanconi anemia (FA) is the most frequent inherited cause of BM failure (BMF). Fifteen FANC genes have been identified to date… Expand
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2008
2008
Although brain development abnormalities and brain cancer predisposition have been reported in some Fanconi patients, the… Expand
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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
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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
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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
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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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