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Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 13, 2017
Genome sequencing and carrier testing: decisions on categorization and whether to disclose results of carrier testingPatricia Himes, Tia L Kauffman, Kristin R Muessig, et al.
Hereditary Cancer in Clinical Practice|January 1, 2020
Recommended care and care adherence following a diagnosis of Lynch syndrome: a mixed-methods studyKathleen F Mittendorf, Jessica Ezzell Hunter, Jennifer L Schneider, et al.
Clinical Case Reports|November 21, 2018
A case for expanding carrier testing to include actionable X-linked disordersAlan F Rope, Tia L Kauffman, Pat Himes, et al.
Health Affairs (Project Hope)|May 8, 2018
Lessons Learned From A Study Of Genomics-Based Carrier Screening For Reproductive Decision MakingBenjamin S Wilfond, Tia L Kauffman, Gail P Jarvik, et al.
American Journal of Medical Genetics. Part A|May 7, 2015
Clinical utility of a next generation sequencing panel assay for Marfan and Marfan-like syndromes featuring aortopathyWhitney Wooderchak-Donahue, Chad VanSant-Webb, Tatiana Tvrdik, et al.
American Journal of Medical Genetics. Part A|January 22, 2016
Patients' ratings of genetic conditions validate a taxonomy to simplify decisions about preconception carrier screening via genome sequencingMichael C Leo, Carmit McMullen, Benjamin S Wilfond, et al.
Familial Cancer|February 8, 2019
Implementation of a Systematic Tumor Screening Program for Lynch Syndrome in an Integrated Health Care SettingElizabeth V Clarke, Kristin R Muessig, Jamilyn Zepp, et al.
American Journal of Human Genetics|May 15, 2018
Preconception Carrier Screening by Genome Sequencing: Results from the Clinical LaboratorySumit Punj, Yassmine Akkari, Jennifer Huang, et al.
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