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Volumn 26, Issue 3, 2000, Pages 362-364
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A common variant in BRCA2 is associated with both breast cancer risk and prenatal viability
a a a b c c d e e f a a b a |
Author keywords
[No Author keywords available]
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Indexed keywords
ADULT;
AGED;
ARTICLE;
BREAST CANCER;
CANCER RISK;
CONTROLLED STUDY;
DISEASE ASSOCIATION;
DNA POLYMORPHISM;
FEMALE;
GENETIC SUSCEPTIBILITY;
GENETIC VARIABILITY;
GENOTYPE;
HUMAN;
MAJOR CLINICAL STUDY;
ONCOGENE;
PRIORITY JOURNAL;
ALLELES;
ANIMALS;
BIRTH WEIGHT;
BRCA2 PROTEIN;
BREAST NEOPLASMS;
CASE-CONTROL STUDIES;
DNA REPAIR;
EXONS;
FEMALE;
FETAL DEATH;
GENE FREQUENCY;
GENES, TUMOR SUPPRESSOR;
GENETIC PREDISPOSITION TO DISEASE;
GENOTYPE;
HUMANS;
INFANT, NEWBORN;
MALE;
MICE;
NEOPLASM PROTEINS;
NEOPLASTIC SYNDROMES, HEREDITARY;
ODDS RATIO;
RISK;
SEX FACTORS;
SEX RATIO;
SINGLE-BLIND METHOD;
TRANSCRIPTION FACTORS;
VARIATION (GENETICS);
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EID: 0033768238
PISSN: 10614036
EISSN: None
Source Type: Journal
DOI: 10.1038/81691 Document Type: Article |
Times cited : (147)
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References (16)
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