Vernooij-van Langen, A M M <br/><br/>
Differences in clinical condition and genotype at time of diagnosis of cystic fibrosis by newborn screening or by symptoms.  [electronic resource] 

 -  Molecular genetics and metabolism   
 - 100-4 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1096-7206 
<br/><br/><label>Standard No.: </label>10.1016/j.ymgme.2014.07.012  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Cystic Fibrosis--diagnosis<br/>Cystic Fibrosis Transmembrane Conductance Regulator--genetics<br/>Gene Frequency<br/>Genotype<br/>Humans<br/>Infant<br/>Infant, Newborn<br/>Mutation<br/>Neonatal Screening--methods<br/>Phenotype<br/>Prevalence<br/>Registries