Molecular approaches for the diagnosis of 21-hydroxylase deficiency and congenital adrenal hyperplasia

Clinics in Laboratory Medicine

Volumn 16, Issue 1, 1996, Pages 125-131

  Wedell, A ^a  

^a KAROLINSKA UNIVERSITY HOSPITAL   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

ALLELE; CONGENITAL ADRENAL HYPERPLASIA; GENE LOCUS; GENE MUTATION; GENETIC ANALYSIS; GENETIC VARIABILITY; GENOTYPE; HUMAN; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; REVIEW; STEROID 21 MONOOXYGENASE DEFICIENCY; TANDEM REPEAT;

EID: 0030009191     PISSN: 02722712     EISSN: None     Source Type: Journal    
DOI: 10.1016/s0272-2712(18)30291-9     Document Type: Review

References (45)

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