Mansfield, E S <br/><br/>
Fluorescent approaches to diagnosis of Lesch-Nyhan syndrome and quantitative analysis of carrier status.  [electronic resource] 

 -  Molecular and cellular probes  Aug 1993 
 - 311-24 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0890-8508 
<br/><br/><label>Standard No.: </label>10.1006/mcpr.1993.1045  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Base Sequence<br/>DNA Primers<br/>Female<br/>Genetic Linkage<br/>Heterozygote<br/>Humans<br/>Hypoxanthine Phosphoribosyltransferase--genetics<br/>Introns--genetics<br/>Lesch-Nyhan Syndrome--diagnosis<br/>Male<br/>Molecular Sequence Data<br/>Multigene Family<br/>Pedigree<br/>Point Mutation--genetics<br/>Polymerase Chain Reaction--methods<br/>Polymorphism, Genetic<br/>Repetitive Sequences, Nucleic Acid--genetics<br/>Sequence Analysis, DNA<br/>Sequence Deletion