Schneider, P M <br/><br/>
Polymorphism of the human complement C4 and steroid 21-hydroxylase genes. Restriction fragment length polymorphisms revealing structural deletions, homoduplications, and size variants.  [electronic resource] 

 -  The Journal of clinical investigation  Sep 1986 
 - 650-7 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0021-9738 
<br/><br/><label>Standard No.: </label>10.1172/JCI112623  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adrenal Hyperplasia, Congenital--genetics<br/>Alleles<br/>Celiac Disease--genetics<br/>Chromosome Aberrations<br/>Chromosome Deletion<br/>Complement C4--genetics<br/>DNA--genetics<br/>DNA Restriction Enzymes<br/>Deoxyribonucleases, Type II Site-Specific<br/>Genes<br/>Haploidy<br/>Humans<br/>Major Histocompatibility Complex<br/>Multiple Sclerosis--genetics<br/>Nucleic Acid Hybridization<br/>Phenotype<br/>Polymorphism, Genetic<br/>Steroid 21-Hydroxylase--genetics<br/>Steroid Hydroxylases--genetics