Improving newborn screening for cystic fibrosis using next-generation sequencing technology: a technical feasibility study.

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From CDC-Authored Genomics Publication Database

This database contains CDC-authored publications in public health genomics including infectious diseases, newborn screening, reproductive health, genetic testing, cancer, chronic diseases, birth defects and developmental disabilities, environmental and occupational health as well as laboratory, bioinformatics and statistical methods.

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• Improving newborn screening for cystic fibrosis using next-generation sequencing technology: a technical feasibility study.  
  Baker Mei W et al. Genet. Med. 2015 Feb 12.
• Implementation of the first worldwide quality assurance program for cystic fibrosis multiple mutation detection in population-based screening.  
  Earley Marie C et al. Clin. Chim. Acta 2011 Jul 15. 412(15-16) 1376-81
• CFTR mutation analysis and haplotype associations in CF patients.  
  Cordovado S K et al. Mol. Genet. Metab. 2012 Feb 105(2) 249-54

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