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Volumn 39, Issue 2, 2007, Pages 159-161
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Fanconi anemia is associated with a defect in the BRCA2 partner PALB2
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Author keywords
[No Author keywords available]
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Indexed keywords
BRCA2 PROTEIN;
COMPLEMENTARY DNA;
GENE PRODUCT;
GENOMIC DNA;
PARTNER AND LOCALIZER OF BRCA2 PROTEIN;
UNCLASSIFIED DRUG;
ARTICLE;
CANCER INHIBITION;
CELL ACTIVITY;
CHROMATIN;
CONGENITAL HEART MALFORMATION;
CROSS LINKING;
DNA REPAIR;
FANCONI ANEMIA;
GENE EXPRESSION;
GENE MUTATION;
GENE SEQUENCE;
GENETIC ASSOCIATION;
GENETIC DISORDER;
GENETIC STABILITY;
GROWTH RETARDATION;
HUMAN;
KAPOSI SARCOMA;
KIDNEY MALFORMATION;
NONSENSE MUTATION;
PHENOTYPE;
PRIORITY JOURNAL;
PROTEIN BINDING;
SKIN MALFORMATION;
THUMB MALFORMATION;
BRCA2 PROTEIN;
BREAST NEOPLASMS;
FANCONI ANEMIA;
FANCONI ANEMIA COMPLEMENTATION GROUP PROTEINS;
GENETIC PREDISPOSITION TO DISEASE;
HUMANS;
MUTATION;
NUCLEAR PROTEINS;
TUMOR SUPPRESSOR PROTEINS;
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EID: 33846601829
PISSN: 10614036
EISSN: 15461718
Source Type: Journal
DOI: 10.1038/ng1942 Document Type: Article |
Times cited : (397)
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References (13)
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