Add to ORKGautosomal recessive disease characterized by pan-cytopenia, congenital malformation and high predis-position to developing malignancies. The phenotypi-cal heterogeneity is associated with genetic hetero-geneity: at least 8 complementation groups (FA-A to FA-H) have been identified, each group presumably corresponding to a separate disease gene (FAA to FAH). The FAA and FAC genes, which account for 75-80 % of the patients, have been cloned. Their protein products have no significant homology to any known protein, or to each other, and may therefore represent elements of a new pathway. This review describes some of the recent contributions to the understand-ing of the molecular basis of FA. Evidence and Information sources. The authors of th
Fanconi anemia (FA) is a rare human recessive syndrome featuring bone marrow failure, myelodysplasia...
SummaryFanconi anemia (FA) is a genetically heterogeneous autosomal recessive disease with bone marr...
Fanconi anemia (FA) is an autosomal recessive disease characterized by progressive pancytopenia, con...
BACKGROUND AND OBJECTIVE: Fanconi anemia (FA) is an autosomal recessive disease characterized by pa...
Fanconi anaemia (FA) is a genetically heterogeneous autosomal recessive disorder associated with chr...
Fanconi anaemia (FA) is a genetically heterogeneous autosomal recessive disorder associated with chr...
Fanconi anemia (FA) is a rare autosomal recessive disease characterized by multiple congenital abnor...
Fanconi anemia (FA) is an autosomal recessive syndrome featuring diverse symptoms including progress...
Abstract Among the chromosome fragility-associated human syndromes that present cancer predispositio...
Fanconi anemia (FA) is a rare genetic disease characterized by congenital malformations, aplastic an...
Fanconi anemia (FA) is a rare genetic disease caused by mutations in genes whose protein products ar...
Fanconi anemia (FA) is a recessively inherited disorder associated with developmental abnormalities,...
SummaryFanconi anemia (FA) is an autosomal recessive chromosomal breakage disorder with diverse clin...
Fanconi anemia is an inherited disease characterized by congenital malformations, pancytopenia, canc...
With many genetic conditions, insights are only now beginning to be attained through molecular appro...
Fanconi anemia (FA) is a rare human recessive syndrome featuring bone marrow failure, myelodysplasia...
SummaryFanconi anemia (FA) is a genetically heterogeneous autosomal recessive disease with bone marr...
Fanconi anemia (FA) is an autosomal recessive disease characterized by progressive pancytopenia, con...
BACKGROUND AND OBJECTIVE: Fanconi anemia (FA) is an autosomal recessive disease characterized by pa...
Fanconi anaemia (FA) is a genetically heterogeneous autosomal recessive disorder associated with chr...
Fanconi anaemia (FA) is a genetically heterogeneous autosomal recessive disorder associated with chr...
Fanconi anemia (FA) is a rare autosomal recessive disease characterized by multiple congenital abnor...
Fanconi anemia (FA) is an autosomal recessive syndrome featuring diverse symptoms including progress...
Abstract Among the chromosome fragility-associated human syndromes that present cancer predispositio...
Fanconi anemia (FA) is a rare genetic disease characterized by congenital malformations, aplastic an...
Fanconi anemia (FA) is a rare genetic disease caused by mutations in genes whose protein products ar...
Fanconi anemia (FA) is a recessively inherited disorder associated with developmental abnormalities,...
SummaryFanconi anemia (FA) is an autosomal recessive chromosomal breakage disorder with diverse clin...
Fanconi anemia is an inherited disease characterized by congenital malformations, pancytopenia, canc...
With many genetic conditions, insights are only now beginning to be attained through molecular appro...
Fanconi anemia (FA) is a rare human recessive syndrome featuring bone marrow failure, myelodysplasia...
SummaryFanconi anemia (FA) is a genetically heterogeneous autosomal recessive disease with bone marr...
Fanconi anemia (FA) is an autosomal recessive disease characterized by progressive pancytopenia, con...