Cystic fibrosis newborn screening: the importance of bloodspot sample quality

ECFS best practice guidelines: the 2018 revision

(2018) Carlo Castellani et al.   Journal of Cystic Fibrosis

Newborn blood spot screening for cystic fibrosis with a four-step screening strategy in the Netherlands

(2018) Jeannette E. Dankert-Roelse et al.   Journal of Cystic Fibrosis

Optimization of the French cystic fibrosis newborn screening programme by a centralized tracking process

(2017) Anne Munck et al.   JOURNAL OF MEDICAL SCREENING

Psychosocial Response to Uncertain Newborn Screening Results for Cystic Fibrosis

(2017) Robin Z. Hayeems et al.   JOURNAL OF PEDIATRICS

Diagnosis of Cystic Fibrosis: Consensus Guidelines from the Cystic Fibrosis Foundation

(2017) Philip M. Farrell et al.   JOURNAL OF PEDIATRICS

Cystic Fibrosis Transmembrane Conductance Regulator-Related Metabolic Syndrome and Cystic Fibrosis Screen Positive, Inconclusive Diagnosis

(2017) Clement L. Ren et al.   JOURNAL OF PEDIATRICS

The benefits of newborn screening for cystic fibrosis: The Canadian experience

(2016) D.Y.F. Mak et al.   Journal of Cystic Fibrosis

Newborn screening for cystic fibrosis

(2016) Carlo Castellani et al.   Lancet Respiratory Medicine

Effect of Dried Blood Spot Quality on Newborn Screening Analyte Concentrations and Recommendations for Minimum Acceptance Criteria for Sample Analysis

(2015) R. S. George et al.   CLINICAL CHEMISTRY

Diagnosis of cystic fibrosis in London and South East England before and after the introduction of newborn screening

(2013) MTC Lim et al.   ARCHIVES OF DISEASE IN CHILDHOOD

Technical report: ethical and policy issues in genetic testing and screening of children

(2013) Laine Friedman Ross et al.   GENETICS IN MEDICINE

European best practice guidelines for cystic fibrosis neonatal screening

(2009) Carlo Castellani et al.   Journal of Cystic Fibrosis

The very low penetrance of cystic fibrosis for the R117H mutation: a reappraisal for genetic counselling and newborn screening

(2009) C Thauvin-Robinet et al.   JOURNAL OF MEDICAL GENETICS