Highsmith, W E <br/><br/>
Frequency of the delta Phe508 mutation and correlation with XV.2c/KM-19 haplotypes in an American population of cystic fibrosis patients: results of a collaborative study.  [electronic resource] 

 -  Clinical chemistry  Oct 1990 
 - 1741-6 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0009-9147 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Base Sequence<br/>Chromosome Deletion<br/>Cystic Fibrosis--genetics<br/>Genetic Carrier Screening<br/>Genotype<br/>Haplotypes<br/>Humans<br/>Molecular Sequence Data<br/>Mutation<br/>Nucleic Acid Probes<br/>Phenotype<br/>Phenylalanine--deficiency<br/>Polymerase Chain Reaction<br/>Risk