Wilms' tumor with an apparently balanced translocation t(X;18) resulting in deletion of the WTX gene

Genes Chromosomes and Cancer

Volumn 46, Issue 10, 2007, Pages 909-913

  Han, Moonjoo ^a   Rivera, Miguel N ^a,b   Batten, Julie M ^a   Haber, Daniel A ^b   Dal Cin, Paola ^c   Iafrate, A John ^a  

^a MASSACHUSETTS GENERAL HOSPITAL   (United States)

^b MASSACHUSETTS GENERAL HOSPITAL CANCER CENTER   (United States)

^c BRIGHAM AND WOMEN S HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

PARAFFIN;

ARTICLE; CARCINOGENESIS; CASE REPORT; CHILD; CHILDHOOD CANCER; CHROMOSOME 18; CHROMOSOME TRANSLOCATION; CHROMOSOME XQ; COMPARATIVE GENOMIC HYBRIDIZATION; DNA DETERMINATION; DNA MICROARRAY; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENE FUSION; GENE INACTIVATION; GENE LOCUS; HUMAN; HUMAN TISSUE; MALE; NEPHROBLASTOMA; ONCOGENE; PRIORITY JOURNAL; PROMOTER REGION; TUMOR GROWTH; TUMOR SUPPRESSOR GENE; WTX GENE; X CHROMOSOME;

CHROMOSOMES, HUMAN, PAIR 18; CHROMOSOMES, HUMAN, X; GENE DELETION; GENE EXPRESSION PROFILING; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT, NEWBORN; KARYOTYPING; KIDNEY NEOPLASMS; MALE; NUCLEIC ACID HYBRIDIZATION; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; TRANSLOCATION, GENETIC; TUMOR SUPPRESSOR PROTEINS; WILMS TUMOR;

EID: 34548747407     PISSN: 10452257     EISSN: 10982264     Source Type: Journal    
DOI: 10.1002/gcc.20476     Document Type: Article

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