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Volumn 53, Issue 4, 2000, Pages 419-422
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Characterization of a novel DNA polymorphism in the human CYP21 gene and application for DNA diagnosis of congenital adrenal hyperplasia
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Author keywords
[No Author keywords available]
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Indexed keywords
STEROID 21 MONOOXYGENASE;
ARTICLE;
CLINICAL ARTICLE;
CODOMINANCE;
CONGENITAL ADRENAL HYPERPLASIA;
CONTROLLED STUDY;
DIAGNOSTIC VALUE;
DISEASE ASSOCIATION;
DNA POLYMORPHISM;
DNA SEQUENCE;
GENE FREQUENCY;
GENE LINKAGE DISEQUILIBRIUM;
GENETIC LINKAGE;
HAPLOTYPE;
HUMAN;
PRIORITY JOURNAL;
RESTRICTION FRAGMENT LENGTH POLYMORPHISM;
ADRENAL HYPERPLASIA, CONGENITAL;
CASE-CONTROL STUDIES;
CHROMOSOME MAPPING;
FEMALE;
GENETIC MARKERS;
HETEROZYGOTE;
HUMANS;
MALE;
PEDIGREE;
POLYMORPHISM, GENETIC;
POLYMORPHISM, RESTRICTION FRAGMENT LENGTH;
PREDICTIVE VALUE OF TESTS;
STEROID 21-HYDROXYLASE;
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EID: 0033792620
PISSN: 03000664
EISSN: None
Source Type: Journal
DOI: 10.1046/j.1365-2265.2000.01090.x Document Type: Article |
Times cited : (2)
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References (14)
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