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JAMIA Open|August 6, 2026
Emoji in clinical messaging: results of a focus group studyColin M E Halverson, Haley Echols, Lauren Kang, et al.Journal of Genetic Counseling|September 26, 2019
Patients' willingness to reconsider cancer genetic testing after initially declining: Mention it againColin M E Halverson, Bronson C Wessinger, Ellen W Clayton, et al.Genetics in Medicine Open|February 25, 2025
An evaluation of practices and policies used in genetics clinics across the United States to manage referrals for Ehlers-Danlos and hypermobility syndromesLauren Boucher, Berkley Nestler, Daniel Groepper, et al.Journal of Community Genetics|September 24, 2021
Assessing parental understanding of variant reclassification in pediatric neurology and developmental pediatrics clinicsAmy Margolin, Benjamin M Helm, Kayla Treat, et al.Molecular Syndromology|April 9, 2015
Whole-Exome Sequencing in the Clinic: Lessons from Six Consecutive Cases from the Clinician's PerspectiveAmber Volk, Erin Conboy, Beverly Wical, et al.Ophthalmic Genetics|May 12, 2023
Motivations and expectations of parents seeking genetic testing for their children with ocular genetic diseaseHannah Gage, Leah Wetherill, Katelynn Anderson, et al.Molecular Genetics & Genomic Medicine|April 25, 2020
Patient perspectives on variant reclassification after cancer susceptibility testingColin M E Halverson, Laurie M Connors, Bronson C Wessinger, et al.Seminars in Pediatric Neurology|July 3, 2018
Novel Homozygous Variant in TTC19 Causing Mitochondrial Complex III Deficiency with Recurrent Stroke-Like Episodes: Expanding the PhenotypeErin Conboy, Duygu Selcen, Michael Brodsky, et al.Clinical Genetics|February 12, 2024
Further evidence of involvement of ITSN1 in autosomal dominant neurodevelopmental disorderKhurram Liaqat, Kayla Treat, Theodore E Wilson, et al.American Journal of Nephrology|May 26, 2016
Living Kidney Donors Who Develop Kidney Failure: Excerpts of Their ThoughtsColin M E Halverson, Jackie Y Wang, Michael Poulson, et al.Pageof 7