Whole-genome paired-end analysis confirms remarkable genomic stability of atypical teratoid/rhabdoid tumors

Genes Chromosomes and Cancer

Volumn 52, Issue 10, 2013, Pages 983-985

  Hoell, Jessica I ^a   Gombert, Michael ^a   Bartenhagen, Christoph ^b   Ginzel, Sebastian ^a,c   Husemann, Peter ^a   Felsberg, Jörg ^a,c   Reifenberger, Guido ^a,d   Eggert, Angelika ^e   Dugas, Martin ^b   Schönberger, Stefan ^f   Borkhardt, Arndt ^a,d   Fischer, Ute ^a  

^a Department of Orthopedic Surgery   (Germany)

^b UNIVERSITY OF MÜNSTER   (Germany)

^c Bonn Rhine Sieg University of Applied Sciences   (Germany)

^d GERMAN CANCER RESEARCH CENTER DKFZ   (Germany)

^e UNIVERSITY OF DUISBURG ESSEN   (Germany)

^f UNIVERSITY OF BONN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; GENE SMARCB 1; UNCLASSIFIED DRUG;

CANCER DIAGNOSIS; CANCER PROGNOSIS; CHILDHOOD CANCER; CHROMOSOME 22; CHROMOSOME DELETION; CHROMOSOME NUMBER; COPY NUMBER VARIATION; DNA MODIFICATION; DNA POLYMORPHISM; DNA SEQUENCE; EXOME; GENE EXPRESSION; GENE LOCUS; GENETIC ALGORITHM; GENETIC CODE; GENETIC VARIABILITY; GENOME ANALYSIS; GENOMIC INSTABILITY; HETEROZYGOSITY LOSS; HOSPITAL PATIENT; HUMAN; LETTER; PRIORITY JOURNAL; RHABDOID TUMOR; SINGLE NUCLEOTIDE POLYMORPHISM;

CHROMOSOMAL PROTEINS, NON-HISTONE; DNA-BINDING PROTEINS; FEMALE; HUMANS; MALE; MUTATION; RHABDOID TUMOR; TRANSCRIPTION FACTORS;

EID: 84883053350     PISSN: 10452257     EISSN: 10982264     Source Type: Journal    
DOI: 10.1002/gcc.22092     Document Type: Letter

References (5)

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