Delineation and candidate gene mutation screening of the 18q22 minimal region of deletion in head and neck squamous cell carcinoma

Oncogene

Volumn 21, Issue 32, 2002, Pages 5016-5023

  Blons, Hélène ^a   Laccourreye, Ollivier ^b   Houllier, Anne Marie ^a   Carnot, Françoise ^b   Brasnu, Daniel ^b   Beaune, Philippe ^a   Zucman Rossi, Jessica ^c   Laurent Puig, Pierre ^a  

^a INSERM   (France)

^b HÔPITAL EUROPÉEN GEORGES POMPIDOU   (France)

^c FONDATION JEAN DAUSSET CEPH   (France)

Author keywords

Allelic losses; Chromosome 18; dHPLC; Head and neck neoplasm; Mutations; Tumor suppressor gene

Indexed keywords

ALLELIC EXCLUSION; ARTICLE; CANCER GROWTH; CHROMOSOME 18Q; CHROMOSOME DELETION; CHROMOSOME MAP; CONTROLLED STUDY; DELETION MUTANT; DOWN REGULATION; EXON; EXPRESSED SEQUENCE TAG; GENE CLUSTER; GENE MUTATION; GENETIC ANALYSIS; GENOTYPE; HEAD AND NECK CANCER; HUMAN; HUMAN CELL; HUMAN TISSUE; MICROSATELLITE MARKER; POINT MUTATION; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SOMATIC MUTATION; SQUAMOUS CELL CARCINOMA; TUMOR SUPPRESSOR GENE;

CARCINOMA, SQUAMOUS CELL; CHROMOSOMES, HUMAN, PAIR 18; GENES, TUMOR SUPPRESSOR; HEAD AND NECK NEOPLASMS; HUMANS; SEQUENCE DELETION;

EID: 0037173754     PISSN: 09509232     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.onc.1205626     Document Type: Article

References (32)