Abstract Described by Guido Fanconi almost 100 years ago, Fanconi anemia (FA) is a rare
genetic disease characterized by developmental abnormalities, bone marrow failure (BMF) …

Simple Summary Fanconi anemia (FA) is a genetic disorder that is characterized by bone
marrow failure (BMF), developmental abnormalities, and predisposition to cancer. In this …

Fanconi anemia (FA), the most common inherited bone marrow failure and leukemia
predisposition syndrome, is generally attributed to alterations in DNA damage responses …

Fanconi anemia (FA) is a recessively inherited disease manifesting developmental
abnormalities, bone marrow failure, and increased risk of malignancies. Whereas FA has …

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 …

Fanconi anemia (FA), a recessive syndrome with both autosomal and X‐linked inheritance,
features diverse clinical symptoms, such as progressive bone marrow failure …

Fanconi anemia (FA) is a complex heterogenic disorder of genomic instability, bone marrow
failure, cancer predisposition, and congenital malformations. The FA signaling network …

Fanconi anemia (FA) is a genomic instability disorder, clinically characterized by congenital
abnormalities, progressive bone marrow failure, and predisposition to malignancy. Cells …

Fanconi anemia (FA) is a cancer predisposition disorder characterized by progressive bone
marrow failure, congenital developmental defects, chromosomal abnormalities, and cellular …

Fanconi anemia (FA) is a rare autosomal and X-linked genetic disease characterized by
congenital abnormalities, progressive bone marrow failure (BMF), and increased cancer risk …