FANCONI ANEMIA, COMPLEMENTATION GROUP F

Known as: FANCF 
Fanconi anemia caused by mutations of the FANCF gene. This gene encodes a polypeptide with homology to the prokaryotic RNA-binding protein ROM.
National Institutes of Health

Topic mentions per year

Topic mentions per year

2000-2018
024620002018

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Highly Cited
2009
Highly Cited
2009
Fanconi Anemia (FA) and Bloom's Syndrome (BS) are genetic disorders characterized by overlapping phenotypes, including aberrant… (More)
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2005
2005
Fanconi anemia (FA) is an autosomal recessive disease marked by bone marrow failure, birth defects, and cancer. The FA proteins… (More)
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Highly Cited
2004
Highly Cited
2004
Patients with advanced stage invasive cervical cancer (CC) exhibit highly complex genomic alterations and respond poorly to… (More)
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2004
2004
The Fanconi anemia (FA) protein FANCF is an essential component of a nuclear core complex that protects the genome against… (More)
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2003
2003
Fanconi Anemia (FA) is an autosomal recessive syndrome characterized by congenital abnormalities, progressive bone marrow failure… (More)
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2003
2003
Fanconi anemia (FA) is an autosomal recessive syndrome characterized by progressive bone marrow failure and cancer predisposition… (More)
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2002
2002
Fanconi anemia (FA) is an autosomal recessive disorder of hematopoiesis characterized by hypersensitivity to DNA crosslinkers… (More)
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2001
2001
OBJECTIVE Fanconi anemia (FA) is a human autosomal-recessive cancer susceptibility disorder characterized by multiple congenital… (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
2000
Highly Cited
2000
Fanconi anaemia (FA) is a chromosomal instability syndrome with autosomal recessive inheritance. We have identified the gene… (More)
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