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Volumn 60, Issue 17, 2000, Pages 4729-4734
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Isolation and mapping of a human septin gene to a region on chromosome 17q, commonly deleted in sporadic epithelial ovarian tumors
a
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Author keywords
[No Author keywords available]
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Indexed keywords
COMPLEMENTARY DNA;
DNA;
SEPTIN;
ARTICLE;
CELL CYCLE;
CHROMOSOME 17Q;
CHROMOSOME LOSS;
CYTOKINESIS;
DNA SEQUENCE;
GENE DELETION;
GENE ISOLATION;
GENE MAPPING;
HETEROZYGOSITY LOSS;
HUMAN;
HUMAN TISSUE;
NUCLEOTIDE SEQUENCE;
OVARY TUMOR;
PRIORITY JOURNAL;
SEQUENCE HOMOLOGY;
TUMOR SUPPRESSOR GENE;
AMINO ACID SEQUENCE;
CHROMOSOME DELETION;
CHROMOSOME MAPPING;
CHROMOSOMES, HUMAN, PAIR 17;
CONTIG MAPPING;
DNA MUTATIONAL ANALYSIS;
DNA, COMPLEMENTARY;
DNA, NEOPLASM;
FEMALE;
GENES, TUMOR SUPPRESSOR;
GTP PHOSPHOHYDROLASES;
GTP-BINDING PROTEINS;
HUMANS;
LOSS OF HETEROZYGOSITY;
MOLECULAR SEQUENCE DATA;
OVARIAN NEOPLASMS;
SEQUENCE HOMOLOGY, AMINO ACID;
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EID: 0034282804
PISSN: 00085472
EISSN: None
Source Type: Journal
DOI: None Document Type: Article |
Times cited : (93)
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References (19)
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