An overview of molecular diagnosis of steroid 21-hydroxylase deficiency

Journal of Molecular Diagnostics

Volumn 3, Issue 2, 2001, Pages 49-54

  Keegan, Catherine E ^a   Killeen, Anthony A ^a  

^a UNIVERSITY OF MICHIGAN MEDICAL SCHOOL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALDOSTERONE; ANDROGEN; DNA; HYDROCORTISONE; MINERALOCORTICOID; OLIGONUCLEOTIDE; RESTRICTION ENDONUCLEASE; STEROID 21 MONOOXYGENASE;

ANDROGEN SYNTHESIS; CONGENITAL ADRENAL HYPERPLASIA; CONTROLLED STUDY; DENATURING GRADIENT GEL ELECTROPHORESIS; DNA PROBE; GENE AMPLIFICATION; GENE DELETION; GENE MUTATION; GENETIC LINKAGE; GENETIC SCREENING; HETERODUPLEX ANALYSIS; HUMAN; LIGASE CHAIN REACTION; NEWBORN SCREENING; POLYMERASE CHAIN REACTION; PRENATAL SCREENING; REVIEW; SALT LOSING NEPHRITIS; SINGLE STRAND CONFORMATION POLYMORPHISM; SOUTHERN BLOTTING; STEROID 21 MONOOXYGENASE DEFICIENCY; STEROIDOGENESIS;

EID: 0035003834     PISSN: 15251578     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1525-1578(10)60651-4     Document Type: Review

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