Localization of a novel t(1;7) translocation associated with Wilms' tumor predisposition and skeletal abnormalities

Genes Chromosomes and Cancer

Volumn 17, Issue 3, 1996, Pages 151-155

  Reynolds, Paul A ^a,d   Powlesland, Rachel M ^a   Keen, T Jeffrey ^b   Inglehearn, Chris F ^b   Cunningham, Aimee F ^c   Green, Eric D ^c   Brown, Keith W ^a  

^a Dept Anat Sch Med Sci U   (United Kingdom)

^b UNIVERSITY COLLEGE LONDON   (United Kingdom)

^c NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

^d SCHOOL OF MEDICAL SCIENCES   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

APLASIA; ARTICLE; CHROMOSOMAL LOCALIZATION; CHROMOSOME ANALYSIS; CHROMOSOME TRANSLOCATION 1; CHROMOSOME TRANSLOCATION 7; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN CELL; KIDNEY DEVELOPMENT; NEPHROBLASTOMA; NONHUMAN; PRIORITY JOURNAL; SKELETON MALFORMATION; TUMOR SUPPRESSOR GENE; YEAST ARTIFICIAL CHROMOSOME;

BONE AND BONES; CHROMOSOMES, ARTIFICIAL, YEAST; CHROMOSOMES, HUMAN, PAIR 7; GENES, WILMS TUMOR; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KIDNEY; KIDNEY NEOPLASMS; MALE; TRANSLOCATION, GENETIC; WILMS TUMOR;

EID: 0029855975     PISSN: 10452257     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1098-2264(199611)17:3<151::AID-GCC2>3.0.CO;2-3     Document Type: Article

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