Kerem, E <br/><br/>
The relation between genotype and phenotype in cystic fibrosis--analysis of the most common mutation (delta F508).  [electronic resource] 

 -  The New England journal of medicine  Nov 1990 
 - 1517-22 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>0028-4793 
<br/><br/><label>Standard No.: </label>10.1056/NEJM199011293232203  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Alleles<br/>Child<br/>Child, Preschool<br/>Chlorides--analysis<br/>Chromosomes, Human, Pair 7<br/>Cystic Fibrosis--genetics<br/>Genotype<br/>Growth<br/>Heterozygote<br/>Homozygote<br/>Humans<br/>Infant<br/>Mutation<br/>Pancreas--physiopathology<br/>Phenotype<br/>Respiratory Function Tests<br/>Sweat--chemistry