Rossetti, S <br/><br/>
Detection of mutations in human genes by a new rapid method: cleavage fragment length polymorphism analysis (CFLPA).  [electronic resource] 

 -  Molecular and cellular probes  Apr 1997 
 - 155-60 p.  digital 
<br/><br/> Publication Type: Comparative Study; 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.1996.0085  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Achondroplasia--genetics<br/>Collagen--genetics<br/>Cystic Fibrosis--genetics<br/>Cystic Fibrosis Transmembrane Conductance Regulator--genetics<br/>DNA Mutational Analysis--methods<br/>DNA Restriction Enzymes<br/>DNA, Single-Stranded--metabolism<br/>Fibroblast Growth Factors--genetics<br/>Humans<br/>Nephritis, Hereditary--genetics<br/>Polycystic Kidney, Autosomal Dominant--genetics<br/>Polymerase Chain Reaction<br/>Polymorphism, Restriction Fragment Length<br/>Protein-Tyrosine Kinases<br/>Proteins--genetics<br/>Receptor, Fibroblast Growth Factor, Type 3<br/>Receptors, Fibroblast Growth Factor--genetics<br/>Silver Staining<br/>TRPP Cation Channels