Genome-wide genotyping of acute myeloid leukemia with translocation t(9;11)(p22;q23) reveals novel recurrent genomic alterations

Haematologica

Volumn 99, Issue 8, 2014, Pages

  Kühn, Michael W M ^a   Bullinger, Lars ^a   Gröschel, Stefan ^a   Krönke, Jan ^a   Edelmann, Jennifer ^a   Rücker, Frank G ^a   Eiwen, Karina ^a   Paschka, Peter ^a   Gaidzik, Verena I ^a   Holzmann, Karlheinz ^a   Schlenk, Richard F ^a   Döhner, Hartmut ^a   Döhner, Konstanze ^a  

^a UNIVERSITY OF ULM   (Germany)

Author keywords

Acute myeloid leukemia; Copy number alterations; Genotyping; Novel recurrent genomic alterations; t(9; 11)(p22; q23)

Indexed keywords

KRUPPEL LIKE FACTOR 5; MIXED LINEAGE LEUKEMIA PROTEIN;

ACUTE GRANULOCYTIC LEUKEMIA; CHROMOSOME 13; CHROMOSOME 7; CHROMOSOME REARRANGEMENT; CHROMOSOME TRANSLOCATION; COPY NUMBER VARIATION; FUSION GENE; GAIN OF FUNCTION MUTATION; GENE DELETION; GENE FREQUENCY; GENOTYPING TECHNIQUE; HUMAN; LETTER; NUCLEOTIDE SEQUENCE; SINGLE NUCLEOTIDE POLYMORPHISM; ADULT; CHROMOSOME 11; CHROMOSOME 9; COHORT ANALYSIS; FEMALE; GENE TRANSLOCATION; GENETIC ASSOCIATION; GENETICS; GENOMICS; LEUKEMIA, MYELOID, ACUTE; MALE; PROCEDURES;

ADULT; CHROMOSOMES, HUMAN, PAIR 11; CHROMOSOMES, HUMAN, PAIR 9; COHORT STUDIES; FEMALE; GENOME-WIDE ASSOCIATION STUDY; GENOMICS; HUMANS; LEUKEMIA, MYELOID, ACUTE; MALE; POLYMORPHISM, SINGLE NUCLEOTIDE; TRANSLOCATION, GENETIC;

EID: 84904703755     PISSN: 03906078     EISSN: 15928721     Source Type: Journal    
DOI: 10.3324/haematol.2014.105544     Document Type: Letter

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