Helmberg, A <br/><br/>
Identification of molecular defects causing congenital adrenal hyperplasia by cloning and differential hybridization of polymerase chain reaction-amplified 21-hydroxylase (CYP21) genes.  [electronic resource] 

 -  DNA and cell biology  Jun 1992 
 - 359-68 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1044-5498 
<br/><br/><label>Standard No.: </label>10.1089/dna.1992.11.359  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adrenal Hyperplasia, Congenital--genetics<br/>Base Sequence<br/>Cloning, Molecular<br/>Genes<br/>Haplotypes<br/>Heterozygote<br/>Humans<br/>Molecular Sequence Data<br/>Oligodeoxyribonucleotides--chemistry<br/>Polymerase Chain Reaction<br/>Steroid 21-Hydroxylase--genetics