fanconi anemia complementation group g
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Current methods for detecting mutations in Fanconi anemia (FA)-suspected patients are inefficient and often miss mutations. We… Expand Abstract Fanconi anaemia (FA) is a genetic disease featuring bone marrow failure, proneness to malignancies, and chromosomal… 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