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Volumn 91, Issue 12, 2000, Pages 1241-1249
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Allelic loss of 14q and 22q, NF2 mutation, and genetic instability occur independently of c-kit mutation in gastrointestinal stromal tumor
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Author keywords
Allelic loss; C kit; Gastrointestinal stromal tumor; Genetic instability; NF2
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Indexed keywords
ADULT;
AGED;
ALLELE;
ARTICLE;
CANCER RISK;
CHROMOSOME 14Q;
CHROMOSOME 22Q;
CHROMOSOME ARM;
CHROMOSOME LOSS;
CLINICAL ARTICLE;
CONNECTIVE TISSUE TUMOR;
CONTROLLED STUDY;
EXON;
FEMALE;
FREQUENCY ANALYSIS;
GASTROINTESTINAL TUMOR;
GENE DELETION;
GENE INSERTION;
GENE LOCUS;
GENE MUTATION;
GENETIC STABILITY;
HETEROZYGOSITY LOSS;
HUMAN;
HUMAN TISSUE;
MALE;
MICROSATELLITE INSTABILITY;
MOLECULAR GENETICS;
MUTATION RATE;
NEUROFIBROMATOSIS;
NONSENSE MUTATION;
ONCOGENE C KIT;
POLYMERASE CHAIN REACTION;
PRIORITY JOURNAL;
PROTO ONCOGENE;
RISK ASSESSMENT;
SINGLE STRAND CONFORMATION POLYMORPHISM;
TUMOR SUPPRESSOR GENE;
ADULT;
AGED;
CHROMOSOME MAPPING;
CHROMOSOMES, HUMAN, PAIR 14;
CHROMOSOMES, HUMAN, PAIR 22;
EXONS;
FEMALE;
GASTROINTESTINAL NEOPLASMS;
GENES, NEUROFIBROMATOSIS 2;
GENETIC MARKERS;
HUMANS;
INTESTINAL NEOPLASMS;
LOSS OF HETEROZYGOSITY;
MALE;
MEMBRANE PROTEINS;
MICROSATELLITE REPEATS;
MIDDLE AGED;
MUTATION, MISSENSE;
NEUROFIBROMIN 2;
POLYMERASE CHAIN REACTION;
POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL;
PROTO-ONCOGENE PROTEINS C-KIT;
STOMACH NEOPLASMS;
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EID: 0034525682
PISSN: 09105050
EISSN: None
Source Type: Journal
DOI: 10.1111/j.1349-7006.2000.tb00910.x Document Type: Article |
Times cited : (74)
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References (33)
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