Analysis of chromosome breakpoints in neuroblastoma at sub-kilobase resolution using fine-tiling oligonucleotide array CGH

Genes Chromosomes and Cancer

Volumn 44, Issue 3, 2005, Pages 305-319

  Selzer, Rebecca R ^a   Richmond, Todd A ^a   Pofahl, Nathan J ^a   Green, Roland D ^a   Eis, Peggy S ^a   Nair, Prakash ^c   Brothman, Arthur R ^b   Stallings, Raymond L ^c,d  

^a Roche NimbleGen Inc   (United States)

^b UNIVERSITY OF UTAH SCHOOL OF MEDICINE   (United States)

^c UNIVERSITY OF TEXAS HEALTH SCIENCE CENTER AT SAN ANTONIO   (United States)

^d Mail Code 7784 ^*  (United States)

Author keywords

[No Author keywords available]

Indexed keywords

SPACER DNA;

AMPLICON; ARTICLE; CHROMOSOME 11Q; CHROMOSOME 17Q; CHROMOSOME 3P; CHROMOSOME ANALYSIS; CHROMOSOME BREAKAGE; CHROMOSOME DUPLICATION; CHROMOSOME MAP; COMPARATIVE GENOMIC HYBRIDIZATION; DNA MICROARRAY; GENETIC POLYMORPHISM; GENOME ANALYSIS; HUMAN; HUMAN CELL; NEUROBLASTOMA; OLIGONUCLEOTIDE PROBE; PRIORITY JOURNAL;

CHROMOSOME BREAKAGE; CHROMOSOMES, HUMAN, PAIR 11; CHROMOSOMES, HUMAN, PAIR 17; GENOME, HUMAN; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; NEUROBLASTOMA; NUCLEIC ACID HYBRIDIZATION; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; TRANSLOCATION, GENETIC;

EID: 25844494223     PISSN: 10452257     EISSN: None     Source Type: Journal    
DOI: 10.1002/gcc.20243     Document Type: Article

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