Lee, Hsien-Hsiung <br/><br/>
Duplication of 111 bases in exon 1 of the CYP21 gene is combined with deletion of CYP21P-C4B genes in steroid 21-hydroxylase deficiency.  [electronic resource] 

 -  Molecular genetics and metabolism  Jul 2003 
 - 214-20 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1096-7192 
<br/><br/><label>Standard No.: </label>10.1016/s1096-7192(03)00087-8  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adrenal Hyperplasia, Congenital--enzymology<br/>Alleles<br/>Base Sequence<br/>Complement C4b--genetics<br/>Crossing Over, Genetic<br/>DNA Mutational Analysis<br/>Humans<br/>Mutation--genetics<br/>Polymerase Chain Reaction<br/>Polymorphism, Restriction Fragment Length<br/>Recombinant Fusion Proteins--genetics<br/>Sequence Deletion<br/>Steroid 21-Hydroxylase--genetics