in a new subtype of Fanconi anemia (FA), FA-P. Monoallelic defects in several FA genes are known to confer susceptibility to breast and ovarian cancers. mutant failed to do so. may contribute to the development of breast cancer in very rare cases
Fanconi anemia (FA) is a rare genetic disease characterized by congenital malformations, aplastic an...
Fanconi anemia (FA) is a recessive disorder associated with progressive pancytopenia, multiple devel...
We identified constitutional truncating mutations of the BRCA1-interacting helicase BRIP1 in 9/1,212...
in a new subtype of Fanconi anemia (FA), FA-P. Monoallelic defects in several FA genes are known to...
Fanconi Anemia (FA) is an autosomal recessive syndrome characterized by congenital abnormalities, pr...
PurposeMonoallelic germ-line mutations in the BRCA1/FANCS, BRCA2/FANCD1 and PALB2/FANCN genes confer...
Fanconi anemia (FA) is a genetically heterogeneous disorder with 22 disease-causing genes reported t...
Altres ajuts: MSSSI/FIS PI12/00070PurposeMonoallelic germ-line mutations in the BRCA1/FANCS, BRCA2/F...
Fanconi anemia (FA) is a genetically heterogeneous disorder with 22 disease-causing genes reported t...
Purpose: Monoallelic germ-line mutations in the BRCA1/FANCS, BRCA2/FANCD1 and PALB2/FANCN genes conf...
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...
Fanconi anemia (FA) is caused by biallelic mutations in FA genes. Monoallelic mutations in five of t...
Fanconi anemia (FA) is a rare autosomal recessive cancer susceptibility disorder characterized by ce...
Fanconi anemia is an inherited dis-ease characterized by bone marrow failure, congenital malformatio...
Fanconi anemia (FA) is a rare genetic disease characterized by congenital malformations, aplastic an...
Fanconi anemia (FA) is a recessive disorder associated with progressive pancytopenia, multiple devel...
We identified constitutional truncating mutations of the BRCA1-interacting helicase BRIP1 in 9/1,212...
in a new subtype of Fanconi anemia (FA), FA-P. Monoallelic defects in several FA genes are known to...
Fanconi Anemia (FA) is an autosomal recessive syndrome characterized by congenital abnormalities, pr...
PurposeMonoallelic germ-line mutations in the BRCA1/FANCS, BRCA2/FANCD1 and PALB2/FANCN genes confer...
Fanconi anemia (FA) is a genetically heterogeneous disorder with 22 disease-causing genes reported t...
Altres ajuts: MSSSI/FIS PI12/00070PurposeMonoallelic germ-line mutations in the BRCA1/FANCS, BRCA2/F...
Fanconi anemia (FA) is a genetically heterogeneous disorder with 22 disease-causing genes reported t...
Purpose: Monoallelic germ-line mutations in the BRCA1/FANCS, BRCA2/FANCD1 and PALB2/FANCN genes conf...
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...
Fanconi anemia (FA) is caused by biallelic mutations in FA genes. Monoallelic mutations in five of t...
Fanconi anemia (FA) is a rare autosomal recessive cancer susceptibility disorder characterized by ce...
Fanconi anemia is an inherited dis-ease characterized by bone marrow failure, congenital malformatio...
Fanconi anemia (FA) is a rare genetic disease characterized by congenital malformations, aplastic an...
Fanconi anemia (FA) is a recessive disorder associated with progressive pancytopenia, multiple devel...
We identified constitutional truncating mutations of the BRCA1-interacting helicase BRIP1 in 9/1,212...