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Volumn 297, Issue 5581, 2002, Pages 606-609
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Biallelic inactivation of BRCA2 in Fanconi anemia
a a a a a a a a a a a a a |
Author keywords
[No Author keywords available]
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Indexed keywords
CLONING;
GENES;
HEALTH RISKS;
MUTAGENESIS;
TUMORS;
CELLULAR HYPERSENSITIVITY;
DISEASES;
BRCA1 PROTEIN;
BRCA2 PROTEIN;
MITOMYCIN C;
CANCER;
DNA;
MUTATION;
ARTICLE;
AUTOSOMAL RECESSIVE DISORDER;
CANCER RISK;
CANCER SUSCEPTIBILITY;
CELL LINE;
FANCONI ANEMIA;
GENE INACTIVATION;
GENE MUTATION;
HUMAN;
HUMAN CELL;
MOLECULAR CLONING;
PATHOGENESIS;
PRIORITY JOURNAL;
ALLELES;
AMINO ACID SEQUENCE;
BRCA2 PROTEIN;
CELL LINE;
DNA DAMAGE;
FANCONI ANEMIA;
FEMALE;
FIBROBLASTS;
FRAMESHIFT MUTATION;
GENE SILENCING;
GENES, BRCA1;
GENES, BRCA2;
GENETIC COMPLEMENTATION TEST;
GERM-LINE MUTATION;
HOMOZYGOTE;
HUMANS;
MALE;
MITOMYCIN;
MOLECULAR SEQUENCE DATA;
MUTATION;
PEDIGREE;
PHENOTYPE;
PROTEIN ISOFORMS;
REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION;
RNA, MESSENGER;
TRANSFECTION;
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EID: 18444362122
PISSN: 00368075
EISSN: None
Source Type: Journal
DOI: 10.1126/science.1073834 Document Type: Article |
Times cited : (994)
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References (30)
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