Vesa, J <br/><br/>
A single PCR marker in strong allelic association with the infantile form of neuronal ceroid lipofuscinosis facilitates reliable prenatal diagnostics and disease carrier identification.  [electronic resource] 

 -  European journal of human genetics : EJHG  1993 
 - 125-32 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1018-4813 
<br/><br/><label>Standard No.: </label>10.1159/000472399  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alleles<br/>Base Sequence<br/>Carrier State--diagnosis<br/>Female<br/>Finland<br/>Genetic Markers<br/>Humans<br/>Linkage Disequilibrium<br/>Male<br/>Molecular Sequence Data<br/>Neuronal Ceroid-Lipofuscinoses--diagnosis<br/>Polymerase Chain Reaction<br/>Polymorphism, Genetic<br/>Polymorphism, Restriction Fragment Length<br/>Prenatal Diagnosis