Spectrum and significance of variants and mutations in the Fanconi anaemia group G gene in children with sporadic acute myeloid leukaemia

British Journal of Haematology

Volumn 133, Issue 3, 2006, Pages 284-292

  Meyer, Stefan ^a,b   Barber, Lisa M ^b   White, Daniel J ^b   Will, Andrew M ^a   Birch, Jillian M ^b   Kohler, Janice A ^c   Ersfeld, Klaus ^d   Blom, Eric ^e   Joenje, Hans ^e   Eden, Tim O B ^a   Malcolm Taylor, G ^b  

^a MANCHESTER UNIVERSITY NHS FOUNDATION TRUST   (United Kingdom)

^b UNIVERSITY OF MANCHESTER   (United Kingdom)

^c UNIVERSITY OF SOUTHAMPTON   (United Kingdom)

^d UNIVERSITY OF HULL   (United Kingdom)

^e VU UNIVERSITY AMSTERDAM   (Netherlands)

Author keywords

Acute myeloid leukaemia; Childhood; Fanconi; Fanconi anaemia group G gene; Genetic variants

Indexed keywords

GENOMIC DNA;

ACUTE GRANULOCYTIC LEUKEMIA; ALLOGENIC BONE MARROW TRANSPLANTATION; ARTICLE; CHILD; CHILDHOOD LEUKEMIA; CONTROLLED STUDY; CYTOGENETICS; DISEASE COURSE; FANCONI ANEMIA; FANCONI ANEMIA GROUP G GENE; FEMALE; GENE; GENETIC VARIABILITY; HUMAN; HUMAN CELL; INFANT; MAJOR CLINICAL STUDY; MALE; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SINGLE STRAND CONFORMATION POLYMORPHISM;

ACUTE DISEASE; ADOLESCENT; AMINO ACID SEQUENCE; ANIMALS; CHILD; CHILD, PRESCHOOL; DNA, NEOPLASM; FANCONI ANEMIA; FANCONI ANEMIA COMPLEMENTATION GROUP G PROTEIN; FEMALE; HUMANS; INFANT; LEUKEMIA, MYELOID; MALE; MOLECULAR SEQUENCE DATA; MUTATION; POLYMERASE CHAIN REACTION; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; SEQUENCE ALIGNMENT;

EID: 33645453358     PISSN: 00071048     EISSN: 13652141     Source Type: Journal    
DOI: 10.1111/j.1365-2141.2006.05985.x     Document Type: Article

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