Condition: FANCONI ANEMIA, COMPLEMENTATION GROUP B
rs1569083185
in
FANCB
gene and
FANCONI ANEMIA, COMPLEMENTATION GROUP B
PMID 21910217
2011 X-linked VACTERL with hydrocephalus syndrome: further delineation of the phenotype caused by FANCB mutations.
PMID 15502827
2004 X-linked inheritance of Fanconi anemia complementation group B.
PMID 17924555
2008 Genetic subtyping of Fanconi anemia by comprehensive mutation screening.
PMID 16679491
2006 Fanconi anaemia complementation group B presenting as X linked VACTERL with hydrocephalus syndrome.