Sinnott, P J <br/><br/>
21-hydroxylase deficiency families with HLA identical affected and unaffected sibs.  [electronic resource] 

 -  Journal of medical genetics  Jan 1989 
 - 10-7 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0022-2593 
<br/><br/><label>Standard No.: </label>10.1136/jmg.26.1.10  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adrenal Hyperplasia, Congenital--genetics<br/>Child<br/>Chromosome Mapping<br/>Complement C4--genetics<br/>Female<br/>HLA Antigens--genetics<br/>HLA-B Antigens--genetics<br/>Haplotypes<br/>Humans<br/>Pedigree<br/>Steroid Hydroxylases--deficiency