fanconi anemia complementation group g

Current methods for detecting mutations in Fanconi anemia (FA)-suspected patients are inefficient and often miss mutations. We… Expand

Fanconi anemia (FA) is the most frequent inherited cause of BM failure (BMF). Fifteen FANC genes have been identified to date… Expand

Although brain development abnormalities and brain cancer predisposition have been reported in some Fanconi patients, the… Expand

Bladder carcinomas frequently show extensive deletions of chromosomes 9p and/or 9q, potentially including the loci of the Fanconi… Expand

BACKGROUND & AIMS How specifically to treat pancreatic and other cancers harboring Fanconi anemia gene mutations has raised great… Expand

Patients with Fanconi anemia (FA) display a wide variety of defects including bone marrow failure and a high risk of developing… Expand

Fanconi anaemia (FA) is an autosomal recessive genetic disorder characterized by progressive bone marrow failure, multiple… Expand

Fanconi anemia (FA) is a genetically heterogeneous autosomal recessive syndrome associated with chromosomal instability… Expand

Fanconi anemia (FA) is a genetic disorder that leads to aplastic anemia and birth defects and predisposes to cancer. FA cells… Expand

Fanconi anemia (FA) is a recessively inherited disease characterized at the cellular level by spontaneous chromosomal instability… Expand