Noninvasive Prenatal Diagnosis for Cystic Fibrosis: Implementation, Uptake, Outcome, and Implications. Chandler Natalie J et al. Clinical chemistry 2019 Sep

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Last Posted: Oct 03, 2019

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• Noninvasive Prenatal Diagnosis for Cystic Fibrosis: Implementation, Uptake, Outcome, and Implications.
  Chandler Natalie J et al. Clinical chemistry 2019 Sep
• Practice variation of genetic counselor engagement in the cystic fibrosis newborn screen-positive diagnostic resolution process.
  Langfelder-Schwind Elinor et al. Journal of genetic counseling 2019 Sep
• [Polygenic risk prediction of common diseases: from epidemiology to clinical application].
  Jansen Philip R et al. Nederlands tijdschrift voor geneeskunde 2019 Sep 163
• Newborn cystic fibrosis screening in southeastern Mexico: Birth prevalence and novel CFTR gene variants.
  Ibarra-González Isabel et al. Journal of medical screening 2018 25(3) 119-125
• Newborn screening to identify cystic fibrosis.
  et al. Nursing children and young people 2017 Feb 29(1) 19
• Pediatric and Adult Recommendations Vary for Sibling Testing in Cystic Fibrosis.
  Brown Kimberly L et al. Journal of genetic counseling 2018 27(5) 1049-1054
• Variations in prenatal screening in a US federal healthcare system: Same coverage, different options.
  Thagard Andrew S et al. Journal of genetic counseling 2019 Sep
• Cystic Fibrosis Mutation Spectrum in North Macedonia: A Step Toward Personalized Therapy.
  Terzic M et al. Balkan journal of medical genetics : BJMG 2019 Jun 22(1) 35-40
• Predictive value of genomic screening: cross-sectional study of cystic fibrosis in 50,788 electronic health records.
  Sugunaraj J P et al. NPJ genomic medicine 2019 421
• Thirtieth Anniversary of Cystic Fibrosis Gene Discovery
  Francis Collins, NIH Director's blog, August 2019

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