Morel, Y <br/><br/>
Rearrangements and point mutations of P450c21 genes are distinguished by five restriction endonuclease haplotypes identified by a new probing strategy in 57 families with congenital adrenal hyperplasia.  [electronic resource] 

 -  The Journal of clinical investigation  Feb 1989 
 - 527-36 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/JCI113914  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adrenal Hyperplasia, Congenital--genetics<br/>Alleles<br/>Chromosome Deletion<br/>Cytochrome P-450 Enzyme System--genetics<br/>DNA Probes<br/>Family<br/>Haploidy<br/>Humans<br/>Mutation<br/>Nucleotide Mapping<br/>Pedigree