Fanconi anemia is a genetic disorder resulting from biallelic mutations in one of the 17 FANC genes. It is characterized by congenital abnormalities, bone marrow failure, and cancer predisposition. The underlying cause is genomic instability resulting from the deficiency in replication-dependent DNA interstrand crosslink repair pathway commonly referred to as the Fanconi anemia-BRCA pathway. This SnapShot presents the key factors involved
Fanconi anemia (FA) is a rare autosomal recessive disease characterized by multiple congenital abnor...
Fanconi anemia is a rare, cancer-prone disease with mutations in 22 genes. The primary defect result...
Fanconi's anemia is a rare autosomal recessive disease characterized by congenital abnormalities, a ...
Fanconi anemia (FA) is a rare genetic disease caused by mutations in genes whose protein products ar...
Fanconi anemia (FA) is a rare autosomal and X-linked genetic disease characterized by congenital abn...
Mutations in any of at least sixteen FANC genes (FANCA–Q) cause Fanconi anemia, a disorder character...
Mutations in any of at least sixteen FANC genes (FANCA-Q) cause Fanconi anemia, a disorder character...
Fanconi anemia (FA) is a recessively inherited disorder associated with developmental abnormalities,...
Fanconi anemia (FA) is a hereditary chromosomal instability disorder often displaying congenital abn...
Abstract. Fanconi anemia (FA), a recessive syndrome with both autosomal and X-linked inheritance, fe...
Fanconi anemia (FA) is a rare human recessive syndrome featuring bone marrow failure, myelodysplasia...
BACKGROUND AND OBJECTIVE: Fanconi anemia (FA) is an autosomal recessive disease characterized by pa...
Fanconi anemia (FA) is an inherited disease distinct from the failure of bone marrow, growth disturb...
With many genetic conditions, insights are only now beginning to be attained through molecular appro...
Copyright © 2012 Najim Ameziane et al. This is an open access article distributed under the Creative...
Fanconi anemia (FA) is a rare autosomal recessive disease characterized by multiple congenital abnor...
Fanconi anemia is a rare, cancer-prone disease with mutations in 22 genes. The primary defect result...
Fanconi's anemia is a rare autosomal recessive disease characterized by congenital abnormalities, a ...
Fanconi anemia (FA) is a rare genetic disease caused by mutations in genes whose protein products ar...
Fanconi anemia (FA) is a rare autosomal and X-linked genetic disease characterized by congenital abn...
Mutations in any of at least sixteen FANC genes (FANCA–Q) cause Fanconi anemia, a disorder character...
Mutations in any of at least sixteen FANC genes (FANCA-Q) cause Fanconi anemia, a disorder character...
Fanconi anemia (FA) is a recessively inherited disorder associated with developmental abnormalities,...
Fanconi anemia (FA) is a hereditary chromosomal instability disorder often displaying congenital abn...
Abstract. Fanconi anemia (FA), a recessive syndrome with both autosomal and X-linked inheritance, fe...
Fanconi anemia (FA) is a rare human recessive syndrome featuring bone marrow failure, myelodysplasia...
BACKGROUND AND OBJECTIVE: Fanconi anemia (FA) is an autosomal recessive disease characterized by pa...
Fanconi anemia (FA) is an inherited disease distinct from the failure of bone marrow, growth disturb...
With many genetic conditions, insights are only now beginning to be attained through molecular appro...
Copyright © 2012 Najim Ameziane et al. This is an open access article distributed under the Creative...
Fanconi anemia (FA) is a rare autosomal recessive disease characterized by multiple congenital abnor...
Fanconi anemia is a rare, cancer-prone disease with mutations in 22 genes. The primary defect result...
Fanconi's anemia is a rare autosomal recessive disease characterized by congenital abnormalities, a ...
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