Last Posted: May 31, 2018
- Reporting incidental findings of genomic disorder-associated copy number variants to unselected biobank participants.
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Di Resta Chiara et al. EJIFCC 2018 Apr 29(1) 4-14 - A comparison of Australian and French families affected by sarcoma: perceptions of genetics and incidental findings.
Rasmussen Victoria et al. Personalized medicine 2018 Jan 15(1) 13-24 - Genetic Counselors' Experience with and Opinions on the Management of Newborn Screening Incidental Carrier Findings.
Leppert Kristen et al. Journal of genetic counseling 2018 Apr - Is it research or is it clinical? Revisiting an old frontier through the lens of next-generation sequencing technologies.
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Franceschini Nora et al. American journal of kidney diseases : the official journal of the National Kidney Foundation 2018 Apr - Genomic sequencing identifies secondary findings in a cohort of parent study participants
ML Thompson et al, Genetics in Medicine, Apr 11, 2018 - Incidental and clinically actionable genetic variants in 1005 whole exomes and genomes from Qatar.
Jain Abhinav et al. Molecular genetics and genomics : MGG 2018 Mar - Practice guideline: joint CCMG-SOGC recommendations for the use of chromosomal microarray analysis for prenatal diagnosis and assessment of fetal loss in Canada.
Armour Christine M et al. Journal of medical genetics 2018 Mar - Responses to receipt of incidental findings for familial hypercholesterolemia in adult biobank participants
L Jones et al, JACC, Mar 2018
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