Diagnostic Transitions of Cystic Fibrosis and CRMS Compared After 12 Years of Newborn Screening in California-Reference-Cited by-同舟云学术

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Diagnostic Transitions of Cystic Fibrosis and CRMS Compared After 12 Years of Newborn Screening in California

Published:2024-09 Issue: Volume: Page:114287
ISSN:0022-3476
Container-title:The Journal of Pediatrics
language:en
Short-container-title:The Journal of Pediatrics

Author:

Sciortino Stanley^ORCID,Graham Steve,Bishop Tracey

Publisher

Elsevier BV

Reference35 articles.

1. Cystic Fibrosis Mortality in Childhood. Data from European Cystic Fibrosis Society Patient Registry;Zolin;Int J Environ Res Public Health,2018

2. Genomic sequencing in cystic fibrosis newborn screening: what works best, two-tier predefined CFTR mutation panels or second-tier CFTR panel followed by third-tier sequencing?;Currier;Genet Med,2017

3. Improving the Sensitivity and Positive Predictive Value in a Cystic Fibrosis Newborn Screening Program Using a Repeat Immunoreactive Trypsinogen and Genetic Analysis;Sontag;The Journal of pediatrics,2016

4. Inconclusive diagnosis after a positive newborn bloodspot screening result for cystic fibrosis; clarification of the harmonised international definition;Southern;J Cyst Fibros,2019

5. Diagnosis of Cystic Fibrosis in Screened Populations;Farrell;The Journal of pediatrics,2017

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