Hemizygous deletions of chromosome band 16q24 in Wilms tumor: Detection by fluorescence in situ hybridization

Cancer Genetics and Cytogenetics

Volumn 115, Issue 2, 1999, Pages 100-105

  Shearer, Patricia D ^a   Valentine, Marcus B ^a   Grundy, Paul ^c   Decou, James M ^d   Banavali, Shripad D ^a   Komuro, Hiroaki ^a   Green, Daniel M ^e   Beckwith, J Bruce ^f   Look, A Thomas ^a,b  

^a ST JUDE CHILDREN S RESEARCH HOSPITAL   (United States)

^b UNIVERSITY OF TENNESSEE COLLEGE OF MEDICINE   (United States)

^c CROSS CANCER INSTITUTE   (Canada)

^d YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^e ROSWELL PARK CANCER INSTITUTE   (United States)

^f LOMA LINDA UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ARTICLE; CHILD; CHROMOSOME 16Q; CHROMOSOME BAND; CHROMOSOME DELETION; CLINICAL ARTICLE; DNA POLYMORPHISM; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HETEROZYGOSITY LOSS; HIGH RISK PATIENT; HUMAN; HUMAN CELL; HUMAN TISSUE; INFANT; MALE; NEPHROBLASTOMA; PRIORITY JOURNAL; TUMOR SUPPRESSOR GENE;

CHILD; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 16; DNA, NEOPLASM; FEMALE; HOMOZYGOTE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; KIDNEY NEOPLASMS; LOSS OF HETEROZYGOSITY; MALE; POLYMORPHISM, GENETIC; WILMS TUMOR;

EID: 0032734971     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-4608(99)00093-X     Document Type: Article

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