Add to ORKGFanconi anemia (FA) is an autosomal recessive genetic disease char-acterized by progressive bone marrow failure, susceptibility to cancer and multiple congenital anomalies. There is important clinical varia-bility among patients and the knowledge of factors which might predict outcome would greatly help the decision making regarding the choices of treatment and the appropriate time to start it. Future studies of the possible correlation between specific mutations with specific clinical presentations will provide the answer to one of these factors. At our Center we standardized a rapid and precise screening test using a mismatch PCR assay for a specific mutation (3788-3790del in exon 38 of gene FANCA) in Brazilian FA patients. We present the...
Fanconi anemia (FA) is a rare genetic instability syndrome characterized by developmental defects, b...
Fanconi anemia (FA) is an autosomal recessive disease characterized by progressive pancytopenia, con...
Fanconi anemia (FA) is a rare human recessive syndrome featuring bone marrow failure, myelodysplasia...
Fanconi anemia (FA) is an autosomal recessive genetic disease characterized by progressive bone marr...
BACKGROUND: Fanconi anemia (FA) is a predominantly autosomal recessive disease with wide genetic het...
Fanconi anaemia (FA) is a recessive autosomal disease determined by mutations in genes of at least e...
Fanconi anemia (FA) is a genetically heterogeneous rare autosomal recessive disorder characterized b...
Fanconi anemia (FA) is a rare genetic disease characterized by congenital malformations, aplastic an...
Fanconi anemia is an inherited disease characterized by congenital malformations, pancytopenia, canc...
A Anemia de Fanconi (AF) é uma doença que apresenta herança autossômica recessiva. É caracterizada p...
A Anemia de Fanconi (AF) é uma doença caracterizada por múltiplas anomalias congênitas, progressiva ...
Fanconi anemia (FA) is a rare autosomal recessive disease characterized by multiple congenital abnor...
Fanconi Anemia (FA) is a rare recessive disorder clinically characterized by progressive bone marrow...
Fanconi anemia (FA) is a rare genetic disease caused by mutations in genes whose protein products ar...
Fanconi anemia (FA) is a rare disease, with an estimated frequency of 1 to 5 per 1,000,000 births, w...
Fanconi anemia (FA) is a rare genetic instability syndrome characterized by developmental defects, b...
Fanconi anemia (FA) is an autosomal recessive disease characterized by progressive pancytopenia, con...
Fanconi anemia (FA) is a rare human recessive syndrome featuring bone marrow failure, myelodysplasia...
Fanconi anemia (FA) is an autosomal recessive genetic disease characterized by progressive bone marr...
BACKGROUND: Fanconi anemia (FA) is a predominantly autosomal recessive disease with wide genetic het...
Fanconi anaemia (FA) is a recessive autosomal disease determined by mutations in genes of at least e...
Fanconi anemia (FA) is a genetically heterogeneous rare autosomal recessive disorder characterized b...
Fanconi anemia (FA) is a rare genetic disease characterized by congenital malformations, aplastic an...
Fanconi anemia is an inherited disease characterized by congenital malformations, pancytopenia, canc...
A Anemia de Fanconi (AF) é uma doença que apresenta herança autossômica recessiva. É caracterizada p...
A Anemia de Fanconi (AF) é uma doença caracterizada por múltiplas anomalias congênitas, progressiva ...
Fanconi anemia (FA) is a rare autosomal recessive disease characterized by multiple congenital abnor...
Fanconi Anemia (FA) is a rare recessive disorder clinically characterized by progressive bone marrow...
Fanconi anemia (FA) is a rare genetic disease caused by mutations in genes whose protein products ar...
Fanconi anemia (FA) is a rare disease, with an estimated frequency of 1 to 5 per 1,000,000 births, w...
Fanconi anemia (FA) is a rare genetic instability syndrome characterized by developmental defects, b...
Fanconi anemia (FA) is an autosomal recessive disease characterized by progressive pancytopenia, con...
Fanconi anemia (FA) is a rare human recessive syndrome featuring bone marrow failure, myelodysplasia...