Cystic fibrosis newborn screening: shifting the key question from "should we screen?" to "how should we screen?"
- PMID: 15173512
- DOI: 10.1542/peds.113.6.1811
Cystic fibrosis newborn screening: shifting the key question from "should we screen?" to "how should we screen?"
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Population-based newborn screening for genetic disorders when multiple mutation DNA testing is incorporated: a cystic fibrosis newborn screening model demonstrating increased sensitivity but more carrier detections.Pediatrics. 2004 Jun;113(6):1573-81. doi: 10.1542/peds.113.6.1573. Pediatrics. 2004. PMID: 15173476
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