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Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 21, 2017
The who, what, and why of research participants' intentions to request a broad range of secondary findings in a diagnostic genomic sequencing studyChristine Rini, Cynthia M Khan, Elizabeth Moore, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 22, 2018
Factors influencing NCGENES research participants' requests for non-medically actionable secondary findingsMyra I Roche, Ida Griesemer, Cynthia M Khan, et al.
Human Molecular Genetics|July 4, 2019
Selective serotonin reuptake inhibitors ameliorate MEGF10 myopathyMadhurima Saha, Skylar A Rizzo, Manashwi Ramanathan, et al.
Physical & Occupational Therapy in Pediatrics|October 31, 2022
The Burden of COVID-19 on Caregivers of Children with Suspected Genetic Conditions: A Therapeutic OdysseyMargaret Waltz, Courtney Canter, Jeannette T Bensen, et al.
NPJ Genomic Medicine|December 17, 2019
FDA oversight of NSIGHT genomic research: the need for an integrated systems approach to regulationLaura V Milko, Flavia Chen, Kee Chan, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 17, 2008
Microduplications of 22q11.2 are frequently inherited and are associated with variable phenotypesZhishuo Ou, Jonathan S Berg, Hagith Yonath, et al.
European Heart Journal Open|December 19, 2024
Older women with non-ST-elevation acute coronary syndrome undergoing invasive or conservative management: an individual patient data meta-analysisFrancesca Rubino, Graziella Pompei, Gregory B Mills, et al.
Clinical Microbiology and Infection : the Official Publication of the European Society of Clinical Microbiology and Infectious Diseases|January 14, 2017
Norwegian patients and retail chicken meat share cephalosporin-resistant Escherichia coli and IncK/blaCMY-2 resistance plasmidsE S Berg, A L Wester, J Ahrenfeldt, et al.
BMC Bioinformatics|July 21, 2021
Pre-capture multiplexing provides additional power to detect copy number variation in exome sequencingDayne L Filer, Fengshen Kuo, Alicia T Brandt, et al.
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