Inherited FANCD1/BRCA2 exon 7 splice mutations associated with acute myeloid leukaemia in Fanconi anaemia D1 are not found in sporadic childhood leukaemia [3]

British Journal of Haematology

Volumn 130, Issue 5, 2005, Pages 796-797

  Barber, Lisa M ^a   Barlow, Rosemary A ^a   Meyer, Stefan ^a,b   White, Daniel J ^a   Will, Andrew M ^b   Eden, Tim O B ^b   Taylor, G Malcolm ^a  

^a UNIVERSITY OF MANCHESTER   (United Kingdom)

^b MANCHESTER UNIVERSITY NHS FOUNDATION TRUST   (United Kingdom)

Author keywords

FANCD1 BRCA2; Fanconi anaemia; Genomic DNA; Leukaemia; Mutation

Indexed keywords

BRCA2 PROTEIN; GENOMIC DNA; FANCD2 PROTEIN, HUMAN; FANCONI ANEMIA GROUP D2 PROTEIN; NUCLEAR PROTEIN;

ACUTE GRANULOCYTIC LEUKEMIA; ALLELE; CANCER RISK; CORRELATION ANALYSIS; DNA DAMAGE; DNA EXTRACTION; DNA FLANKING REGION; EXON; FANCONI ANEMIA; GENE AMPLIFICATION; GENE MUTATION; GENOTYPE; HEMATOLOGIC MALIGNANCY; HUMAN; LETTER; LEUKEMIA; MEDICAL LITERATURE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RISK ASSESSMENT; RNA SPLICING; UNITED KINGDOM; ACUTE DISEASE; ACUTE LYMPHOCYTIC LEUKEMIA; ALTERNATIVE RNA SPLICING; CHILD; DISEASE PREDISPOSITION; GENETICS; INFANT; MYELOID LEUKEMIA; PRESCHOOL CHILD; TUMOR SUPPRESSOR GENE;

ACUTE DISEASE; ALTERNATIVE SPLICING; CHILD; CHILD, PRESCHOOL; DISEASE SUSCEPTIBILITY; EXONS; FANCONI ANEMIA; FANCONI ANEMIA COMPLEMENTATION GROUP D2 PROTEIN; GENES, BRCA2; HUMANS; INFANT; LEUKEMIA, LYMPHOCYTIC, ACUTE, L1; LEUKEMIA, MYELOID; NUCLEAR PROTEINS;

EID: 27244442927     PISSN: 00071048     EISSN: 13652141     Source Type: Journal    
DOI: 10.1111/j.1365-2141.2005.05677.x     Document Type: Letter

References (6)

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