Narzi, L <br/><br/>
Does cystic fibrosis neonatal screening detect atypical CF forms? Extended genetic characterization and 4-year clinical follow-up.  [electronic resource] 

 -  Clinical genetics  Jul 2007 
 - 39-46 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0009-9163 
<br/><br/><label>Standard No.: </label>10.1111/j.1399-0004.2007.00825.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Child, Preschool<br/>Cystic Fibrosis--diagnosis<br/>Cystic Fibrosis Transmembrane Conductance Regulator--genetics<br/>Follow-Up Studies<br/>Genetic Testing<br/>Genotype<br/>Heterozygote<br/>Humans<br/>Infant<br/>Infant, Newborn<br/>Neonatal Screening<br/>Trypsin--blood<br/>Trypsinogen--blood