Fanconi anemia is an inherited dis-ease characterized by bone marrow failure, congenital malformations, and predisposition to cancer. The breast cancer susceptibility gene BRCA2 was recently found to be as-sociated with Fanconi anemia comple-mentation group D1 (FA-D1). We ex-amined four kindreds afflicted with Fanconi anemia for the presence of germline BRCA2 mutations. One kin-dred, of Ashkenazi Jewish ancestry, had five members who were diag-nosed with breast cancer and two cousins who were BRCA2*6174delT
Fanconi anemia (FA) is a genetically heterogeneous disorder with 22 disease-causing genes reported t...
ABSTRACT- The hypothesis that heterozygotes for the Fanconi anemia (FA) gene are predisposed to canc...
Fanconi anemia (FA) is a rare genetic disease caused by mutations in genes whose protein products ar...
Fanconi Anemia (FA) is an autosomal recessive syndrome characterized by congenital abnormalities, pr...
Fanconi anemia (FA) is a rare autosomal recessive cancer susceptibility disorder characterized by ce...
Fanconi anemia (FA) is a genetically heterogeneous disorder with 22 disease-causing genes reported t...
Fanconi anaemia (FA) is a rare recessive disorder associated with chromosomal fragility, aplastic an...
Fanconi anemia (FA) is a genetically heterogeneous disorder with 22 disease-causing genes reported t...
PurposeMonoallelic germ-line mutations in the BRCA1/FANCS, BRCA2/FANCD1 and PALB2/FANCN genes confer...
Fanconi anemia (FA) is a rare genetic disorder caused by pathogenic variants (PV) in at least 22 gen...
Fanconi anaemia (FA) is an inherited chromosomal instability disorder characterised by congenital an...
Altres ajuts: MSSSI/FIS PI12/00070PurposeMonoallelic germ-line mutations in the BRCA1/FANCS, BRCA2/F...
Fanconi anemia (FA) is a rare autosomal recessive disease characterized by multiple congenital abnor...
in a new subtype of Fanconi anemia (FA), FA-P. Monoallelic defects in several FA genes are known to...
Purpose: Monoallelic germ-line mutations in the BRCA1/FANCS, BRCA2/FANCD1 and PALB2/FANCN genes conf...
Fanconi anemia (FA) is a genetically heterogeneous disorder with 22 disease-causing genes reported t...
ABSTRACT- The hypothesis that heterozygotes for the Fanconi anemia (FA) gene are predisposed to canc...
Fanconi anemia (FA) is a rare genetic disease caused by mutations in genes whose protein products ar...
Fanconi Anemia (FA) is an autosomal recessive syndrome characterized by congenital abnormalities, pr...
Fanconi anemia (FA) is a rare autosomal recessive cancer susceptibility disorder characterized by ce...
Fanconi anemia (FA) is a genetically heterogeneous disorder with 22 disease-causing genes reported t...
Fanconi anaemia (FA) is a rare recessive disorder associated with chromosomal fragility, aplastic an...
Fanconi anemia (FA) is a genetically heterogeneous disorder with 22 disease-causing genes reported t...
PurposeMonoallelic germ-line mutations in the BRCA1/FANCS, BRCA2/FANCD1 and PALB2/FANCN genes confer...
Fanconi anemia (FA) is a rare genetic disorder caused by pathogenic variants (PV) in at least 22 gen...
Fanconi anaemia (FA) is an inherited chromosomal instability disorder characterised by congenital an...
Altres ajuts: MSSSI/FIS PI12/00070PurposeMonoallelic germ-line mutations in the BRCA1/FANCS, BRCA2/F...
Fanconi anemia (FA) is a rare autosomal recessive disease characterized by multiple congenital abnor...
in a new subtype of Fanconi anemia (FA), FA-P. Monoallelic defects in several FA genes are known to...
Purpose: Monoallelic germ-line mutations in the BRCA1/FANCS, BRCA2/FANCD1 and PALB2/FANCN genes conf...
Fanconi anemia (FA) is a genetically heterogeneous disorder with 22 disease-causing genes reported t...
ABSTRACT- The hypothesis that heterozygotes for the Fanconi anemia (FA) gene are predisposed to canc...
Fanconi anemia (FA) is a rare genetic disease caused by mutations in genes whose protein products ar...