NEWBORN SCREENING
Last Updated: Sep 15, 2016
- A secondary benefit: the reproductive impact of carrier results from newborn screening for cystic fibrosis.
Bombard Yvonne et al. Genetics in medicine : official journal of the American College of Medical Genetics 2016 Sep - Ethical issues in pediatric genetic testing and screening.
Botkin Jeffrey R et al. Current opinion in pediatrics 2016 Sep - Lab Quality Program Important to Newborn Screening
- Prevalence of Sickle Cell Trait and Reliability of Self-Reported Status among Expectant Parents in Nigeria: Implications for Targeted Newborn Screening.
Burnham-Marusich Amanda R et al. Public health genomics 2016 Sep 19(5) - Beyond the Blood Spot: Newborn Screening for Hearing Loss and Critical Congenital Heart Disease
CDC Public Health Grand Rounds, Septemeber 20, 2016 - A Population-Based Genomic Study of Inherited Metabolic Diseases Detected Through Newborn Screening.
Park Kyoung Jin et al. Annals of laboratory medicine 2016 Nov 36(6) 561-72 - Biobank participant support of newborn screening for disorders with variable treatment and intervention options.
Bunnell Megan E et al. Journal of community genetics 2016 Sep - Mothers' Views on Longer Storage of Neonatal Dried Blood Spots for Specific Secondary Uses.
van Teeffelen Sarah R et al. Public health genomics 2016 19(1) 25-33 - Long-term follow-up in newborn screening: the role of collaboration.
Wasserstein Melissa P et al. Genetics in medicine : official journal of the American College of Medical Genetics 2016 Aug - Long-term follow-up in newborn screening: the role of collaboration
MP Wassertein, Genetics in Medicine, AUgust 25, 2016 - Dataset and standard operating procedure for newborn screening of six lysosomal storage diseases: By tandem mass spectrometry.
Elliott Susan et al. Data in brief 2016 Sep 8915-24 - Development of carrier testing for common inborn errors of metabolism in the Wisconsin Plain population.
Kuhl Ashley et al. Genetics in medicine : official journal of the American College of Medical Genetics 2016 Aug - Parental intentions to enroll children in a voluntary expanded newborn screening program.
Paquin Ryan S et al. Social science & medicine (1982) 2016 Jul 16617-24 - High prevalence of DUOX2 gene mutations among children with congenital hypothyroidism in central China.
Jiang Hong, et al. European journal of medical genetics 2016 8 - Parent Experience With False-Positive Newborn Screening Results for Cystic Fibrosis.
Hayeems Robin Z et al. Pediatrics 2016 Aug
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