Fält, S <br/><br/>
Identification of in vivo mutations in exon 5 of the human HPRT gene in a set of pooled T-cell mutants by constant denaturant capillary electrophoresis (CDCE).  [electronic resource] 

 -  Mutation research  Jul 2000 
 - 57-66 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>0027-5107 
<br/><br/><label>Standard No.: </label>10.1016/s0027-5107(00)00046-4  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Base Sequence<br/>DNA--chemistry<br/>DNA Mutational Analysis<br/>Electrophoresis, Capillary--methods<br/>Exons--genetics<br/>Humans<br/>Hypoxanthine Phosphoribosyltransferase--genetics<br/>Male<br/>Mutation<br/>Nucleic Acid Denaturation<br/>Point Mutation<br/>Sensitivity and Specificity<br/>T-Lymphocytes--cytology<br/>Temperature