Add to ORKGAbstract. Fanconi anemia (FA), a recessive syndrome with both autosomal and X-linked inheritance, features diverse clinical symptoms, such as progressive bone marrow failure, hypersensitivity to DNA cross-linking agents, chromosomal instability an
Copyright © 2012 Laura E. Hays et al. This is an open access article distributed under the Creative ...
With many genetic conditions, insights are only now beginning to be attained through molecular appro...
Fanconi anemia is an inherited disease characterized by genomic instability, hypersensitivity to DNA...
Fanconi anemia (FA) is a rare human recessive syndrome featuring bone marrow failure, myelodysplasia...
Fanconi anemia is a genetic disorder resulting from biallelic mutations in one of the 17 FANC genes....
Fanconi anemia (FA) is a recessively inherited disorder associated with developmental abnormalities,...
Fanconi anemia (FA) is a rare genetic disease caused by mutations in genes whose protein products ar...
Fanconi anemia (FA) is a rare autosomal recessive disease characterized by multiple congenital abnor...
Abstract Among the chromosome fragility-associated human syndromes that present cancer predispositio...
Fanconi anemia (FA) is a rare autosomal and X-linked genetic disease characterized by congenital abn...
Fanconi anemia (FA) is a hereditary chromosomal instability disorder often displaying congenital abn...
Copyright © 2012 Najim Ameziane et al. This is an open access article distributed under the Creative...
Fanconi anemia (FA) is a genetically heterogeneous rare autosomal recessive disorder characterized b...
BACKGROUND AND OBJECTIVE: Fanconi anemia (FA) is an autosomal recessive disease characterized by pa...
Abstract. To identify the gene underlying Fanconi anemia (FA) complementation group I we studied inf...
Copyright © 2012 Laura E. Hays et al. This is an open access article distributed under the Creative ...
With many genetic conditions, insights are only now beginning to be attained through molecular appro...
Fanconi anemia is an inherited disease characterized by genomic instability, hypersensitivity to DNA...
Fanconi anemia (FA) is a rare human recessive syndrome featuring bone marrow failure, myelodysplasia...
Fanconi anemia is a genetic disorder resulting from biallelic mutations in one of the 17 FANC genes....
Fanconi anemia (FA) is a recessively inherited disorder associated with developmental abnormalities,...
Fanconi anemia (FA) is a rare genetic disease caused by mutations in genes whose protein products ar...
Fanconi anemia (FA) is a rare autosomal recessive disease characterized by multiple congenital abnor...
Abstract Among the chromosome fragility-associated human syndromes that present cancer predispositio...
Fanconi anemia (FA) is a rare autosomal and X-linked genetic disease characterized by congenital abn...
Fanconi anemia (FA) is a hereditary chromosomal instability disorder often displaying congenital abn...
Copyright © 2012 Najim Ameziane et al. This is an open access article distributed under the Creative...
Fanconi anemia (FA) is a genetically heterogeneous rare autosomal recessive disorder characterized b...
BACKGROUND AND OBJECTIVE: Fanconi anemia (FA) is an autosomal recessive disease characterized by pa...
Abstract. To identify the gene underlying Fanconi anemia (FA) complementation group I we studied inf...
Copyright © 2012 Laura E. Hays et al. This is an open access article distributed under the Creative ...
With many genetic conditions, insights are only now beginning to be attained through molecular appro...
Fanconi anemia is an inherited disease characterized by genomic instability, hypersensitivity to DNA...