A common region of loss of heterozygosity in Wilms' tumor and embryonal rhabdomyosarcoma distal to the D11S988 locus on chromosome 11p15.5

Human Genetics

Volumn 97, Issue 2, 1996, Pages 163-170

  Besnard Guérin, Corinne ^a,c   Newsham, Irene ^a,b,d   Winqvist, Robert ^a,e   Cavenee, Webster K ^a,b  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b UNIVERSITY OF CALIFORNIA SAN DIEGO   (United States)

^c HÔPITAL NECKER ENFANTS MALADES   (France)

^d UNIVERSITY OF CALIFORNIA   (United States)

^e OULU UNIVERSITY HOSPITAL   (Finland)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL CELL; ARTICLE; BECKWITH WIEDEMANN SYNDROME; CHROMOSOME 11P; CHROMOSOME TRANSLOCATION; CONTROLLED STUDY; EMBRYONAL RHABDOMYOSARCOMA; GENE LOSS; GENE MAPPING; HETEROZYGOSITY LOSS; HUMAN; HUMAN CELL; HUMAN TISSUE; NEPHROBLASTOMA; NONHUMAN; PRIORITY JOURNAL;

BASE SEQUENCE; BECKWITH-WIEDEMANN SYNDROME; CELL LINE; CHILD; CHROMOSOMES, HUMAN, PAIR 11; GENE DELETION; GENES, WILMS TUMOR; GENETIC MARKERS; HETEROZYGOTE; HUMANS; HYBRID CELLS; KIDNEY NEOPLASMS; MOLECULAR SEQUENCE DATA; RHABDOMYOSARCOMA, EMBRYONAL; TRANSLOCATION, GENETIC; WILMS TUMOR;

EID: 0030027206     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/BF02265259     Document Type: Article

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