Constitutional sequence variation in the Fanconi anaemia group C (FANCC) gene in childhood acute myeloid leukaemia

British Journal of Haematology

Volumn 121, Issue 1, 2003, Pages 57-62

  Barber, Lisa M ^a   McGrath, Helen E N ^a   Meyer, Stefan ^a   Will, Andrew M ^a   Birch, Jillian M ^a   Eden, Osborn B ^a   Taylor, G Malcolm ^a  

^a UNIVERSITY OF MANCHESTER   (United Kingdom)

Author keywords

Childhood AML; FANCC; Fanconi anaemia; Genetic susceptibility

Indexed keywords

ACUTE GRANULOCYTIC LEUKEMIA; ACUTE LYMPHOBLASTIC LEUKEMIA; ADOLESCENT; AMINO ACID SUBSTITUTION; ARTICLE; BLOOD SAMPLING; CANCER RISK; CHILD; CONFIDENCE INTERVAL; CONTROLLED STUDY; DNA EXTRACTION; FANCONI ANEMIA; FEMALE; GENE MUTATION; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; HUMAN; INFANT; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; UMBILICAL CORD BLOOD;

ACUTE DISEASE; CASE-CONTROL STUDIES; CELL CYCLE PROTEINS; CHILD; CONFIDENCE INTERVALS; DNA-BINDING PROTEINS; FANCONI ANEMIA; FANCONI ANEMIA COMPLEMENTATION GROUP C PROTEIN; FANCONI ANEMIA COMPLEMENTATION GROUP PROTEINS; FETAL BLOOD; GENETIC PREDISPOSITION TO DISEASE; HUMANS; INFANT, NEWBORN; LEUKEMIA, LYMPHOCYTIC, ACUTE, L1; LEUKEMIA, MYELOID; NUCLEAR PROTEINS; ODDS RATIO; POLYMORPHISM, GENETIC; PROTEINS; RISK;

EID: 0037393869     PISSN: 00071048     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2141.2003.04234.x     Document Type: Article

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