Last Posted: Nov 07, 2019
- Newborn Screening for Inherited Metabolic Disorders: Early Identification and Long-Term Care for Patients in the Plain Community, Wisconsin, 2011-2017.
Held Patrice K et al. Public health reports (Washington, D.C. : 1974) 134(2_suppl) 58S-63S - Creating genetic reports that are understood by nonspecialists: a case study.
Recchia Gabriel et al. Genetics in medicine : official journal of the American College of Medical Genetics 2019 Sep - The wild west of prenatal genetic testing
A Ramchandani, Mashable, August 2019 - Genomic malpractice: what healthcare providers need to know to reduce the risk
J McCarthy, Precision Medicine Advisor, June 10, 2019 - Carrier screening for recessive disorders
S Antonarakis, Nature Reviews Genetics, May 30, 2019 - User Acceptability of Whole Exome Reproductive Carrier Testing for Consanguineous Couples in Australia.
Josephi-Taylor Sarah et al. Journal of genetic counseling 2019 Apr 28(2) 240-250 - Challenging the Current Recommendations for Carrier Testing in Children.
VanNoy Grace E et al. Pediatrics 2019 Jan 143(Suppl 1) S27-S32 - Australians' perspectives on support around use of personal genomic testing: Findings from the Genioz study.
Metcalfe Sylvia A et al. European journal of medical genetics 2018 Nov - Clinical utility of expanded carrier screening: results-guided actionability and outcomes
KA Johansen et al, Genetics in Medicine, October 11, 2018 - What do women (and men) want? Parents weigh in on genetic testing for rare diseases in children
S Grosse, CDC Blog, 2018
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