Condition: FANCONI ANEMIA, COMPLEMENTATION GROUP I
rs140404896
in
FANCI
gene and
FANCONI ANEMIA, COMPLEMENTATION GROUP I
PMID 22720145
2012 Diagnosis of fanconi anemia: mutation analysis by next-generation sequencing.
PMID 26590883
2016 Novel FANCI mutations in Fanconi anemia with VACTERL association.
PMID 24989076
2015 Finnish Fanconi anemia mutations and hereditary predisposition to breast and prostate cancer.
PMID 21324748
2011 First systematic experience of preimplantation genetic diagnosis for de-novo mutations.
PMID 17924555
2008 Genetic subtyping of Fanconi anemia by comprehensive mutation screening.
PMID 17460694
2007 FANCI is a second monoubiquitinated member of the Fanconi anemia pathway.
PMID 17452773
2007 Identification of the Fanconi anemia complementation group I gene, FANCI.
rs121918163
in
POLG;FANCI
gene and
FANCONI ANEMIA, COMPLEMENTATION GROUP I
PMID 17460694
2007 FANCI is a second monoubiquitinated member of the Fanconi anemia pathway.
PMID 17412408
2007 Identification of the FANCI protein, a monoubiquitinated FANCD2 paralog required for DNA repair.
PMID 17452773
2007 Identification of the Fanconi anemia complementation group I gene, FANCI.