Errors in genome sequencing result disclosures: A randomized controlled trial comparing neonatology non-genetics healthcare professionals and genetic counselors-Reference-Cited by-同舟云学术

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Errors in genome sequencing result disclosures: A randomized controlled trial comparing neonatology non-genetics healthcare professionals and genetic counselors

Published:2024-09 Issue:9 Volume:26 Page:101198
ISSN:1098-3600
Container-title:Genetics in Medicine
language:en
Short-container-title:Genetics in Medicine

Author:

Coleman Tanner F.^ORCID,Pugh Jada,Kelley Whitley V.,East Kelly M.,Greve Veronica,Finnila Candice R.,Henson Ava,Korf Bruce R.,Barsh Gregory S.,Cooper Gregory M.,Cochran Meagan E.

Funder

National Human Genome Research Institute

National Institute on Minority Health and Health Disparities

National Cancer Institute

Publisher

Elsevier BV

Reference35 articles.

1. Evidence from 2100 index cases supports genome sequencing as a first-tier genetic test;Guo;Genet Med,2024

2. Exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disability: an evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG);Manickam;Genet Med,2021

3. Whole genome sequencing expands diagnostic utility and improves clinical management in pediatric medicine;Stavropoulos;NPJ Genom Med,2016

4. Genomic diagnosis for children with intellectual disability and/or developmental delay;Bowling;Genome Med,2017

5. Utilization and uptake of clinical genetics services in high-income countries: a scoping review;Dragojlovic;Health Policy,2021

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