Carrera, P <br/><br/>
Rapid detection of 21-hydroxylase deficiency mutations by allele-specific in vitro amplification and capillary zone electrophoresis.  [electronic resource] 

 -  Clinical chemistry  Nov 1997 
 - 2121-7 p.  digital 
<br/><br/> Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0009-9147 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adrenal Hyperplasia, Congenital<br/>Alleles<br/>Benzothiazoles<br/>Diamines<br/>Electrophoresis, Capillary<br/>Female<br/>Fluorescent Dyes<br/>Gene Amplification<br/>Humans<br/>Lasers<br/>Male<br/>Organic Chemicals<br/>Point Mutation<br/>Polymerase Chain Reaction<br/>Quinolines<br/>Reproducibility of Results<br/>Sensitivity and Specificity<br/>Spectrometry, Fluorescence<br/>Steroid 21-Hydroxylase--genetics