Frequent allelic loss at chromosome arm 3p is distinct from genetic alterations of the Von-Hippel Lindau tumor suppressor gene in head and neck cancer

Oncogene

Volumn 12, Issue 2, 1996, Pages 365-369

  Waber, Pamela G ^a   Lee, Norris K ^b   Nisen, Perry D ^a  

^a UNIVERSITY OF TEXAS SOUTHWESTERN MEDICAL CENTER   (United States)

^b UNIVERSITY OF TEXAS SOUTHWESTERN MEDICAL CENTER   (United States)

Author keywords

Chromosome 3; Head and neck cancer; Loss of heterozygosity; Von Hippel Lindau syndrome

Indexed keywords

BIOLOGICAL MARKER;

ARTICLE; CHROMOSOME 3P; CLINICAL ARTICLE; DNA FINGERPRINTING; DNA SEQUENCE; EXON; GENE MUTATION; GENETIC HETEROGENEITY; HEAD AND NECK CANCER; HUMAN; HUMAN TISSUE; PATHOGENESIS; PRIORITY JOURNAL; SQUAMOUS CELL CARCINOMA; TUMOR SUPPRESSOR GENE; VON HIPPEL LINDAU DISEASE;

CARCINOMA, SQUAMOUS CELL; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 3; GENES, TUMOR SUPPRESSOR; HEAD AND NECK NEOPLASMS; HIPPEL-LINDAU DISEASE; HUMANS; METHYLATION; MUTATION; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH;

EID: 0030071144     PISSN: 09509232     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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