An absence of founder BRCA2 mutations in individuals with squamous cell carcinoma of the head and neck [1]

International Journal of Cancer

Volumn 83, Issue 6, 1999, Pages 803-804

  Hamel, N ^a   Manning, A ^a   Black, M J ^a   Tonin, P N ^a   Foulkes, W D ^a  

^a MONTREAL GENERAL HOSPITAL   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

CARCINOGENESIS; CHROMOSOME 13Q; EXON; GENE LOCATION; GENE MUTATION; HEAD AND NECK CANCER; HUMAN; LETTER; PRIORITY JOURNAL; SINGLE STRAND CONFORMATION POLYMORPHISM; SQUAMOUS CELL CARCINOMA; TUMOR SUPPRESSOR GENE;

ADULT; AGED; AGED, 80 AND OVER; BRCA2 PROTEIN; CARCINOMA, SQUAMOUS CELL; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 13; DNA TRANSPOSABLE ELEMENTS; EUROPEAN CONTINENTAL ANCESTRY GROUP; FAMILY; FRANCE; GENES, TUMOR SUPPRESSOR; GENETIC MARKERS; HEAD AND NECK NEOPLASMS; HETEROZYGOTE DETECTION; HUMANS; JEWS; LARYNGEAL NEOPLASMS; LOSS OF HETEROZYGOSITY; MIDDLE AGED; MUTATION; NEOPLASM PROTEINS; QUEBEC; SEQUENCE DELETION; TRANSCRIPTION FACTORS;

EID: 0032706975     PISSN: 00207136     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1097-0215(19991210)83:6<803::AID-IJC17>3.0.CO;2-N     Document Type: Letter

References (14)