Add to ORKGFanconi anemia (FA) is a rare autosomal recessive disease characterized by multiple congenital abnormalities, bone marrow failure and susceptibility to cancer. Fanconi anemia is genetically heterogeneous, with at least eight complementation groups (A±H), each presumably corresponding to a separate disease gene. Recently, the FANCA (Fanconi anemia complementation group A), FANCG and FANCF genes were cloned. The study of the natural history of genotypically different Fanconi anemia patients is important to identify high-risk patients with poor hematological outcome as candidates for frequent monitoring and early bone marro
Fanconi anemia is an inherited disease characterized by congenital malformations, pancytopenia, canc...
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 congenital malformations,...
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,...
Fanconi anemia (FA) is a genetically heterogeneous rare autosomal recessive disorder characterized b...
Fanconi anemia (FA) is a clinically and genetically heterogeneous disorder. Clinical care is complic...
SummaryFanconi anemia (FA) is an autosomal recessive chromosomal breakage disorder with diverse clin...
Fanconi anemia (FA) is a rare human recessive syndrome featuring bone marrow failure, myelodysplasia...
Fanconi anemia (FA) is an autosomal recessive syndrome featuring diverse symptoms including progress...
Abstract Background Fanconi anemia (FA) is an inherited bone marrow failure syndrome associated with...
Fanconi anemia (FA) is a rare genetic disorder caused by pathogenic variants (PV) in at least 22 gen...
Abstract Among the chromosome fragility-associated human syndromes that present cancer predispositio...
Fanconi anemia is an inherited disease characterized by congenital malformations, pancytopenia, canc...
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 congenital malformations,...
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,...
Fanconi anemia (FA) is a genetically heterogeneous rare autosomal recessive disorder characterized b...
Fanconi anemia (FA) is a clinically and genetically heterogeneous disorder. Clinical care is complic...
SummaryFanconi anemia (FA) is an autosomal recessive chromosomal breakage disorder with diverse clin...
Fanconi anemia (FA) is a rare human recessive syndrome featuring bone marrow failure, myelodysplasia...
Fanconi anemia (FA) is an autosomal recessive syndrome featuring diverse symptoms including progress...
Abstract Background Fanconi anemia (FA) is an inherited bone marrow failure syndrome associated with...
Fanconi anemia (FA) is a rare genetic disorder caused by pathogenic variants (PV) in at least 22 gen...
Abstract Among the chromosome fragility-associated human syndromes that present cancer predispositio...
Fanconi anemia is an inherited disease characterized by congenital malformations, pancytopenia, canc...
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...