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Genome Biology|September 17, 2011
The promise and limitations of population exomics for human evolution studiesJacob A Tennessen, Timothy D O'Connor, Michael J Bamshad, et al.American Journal of Human Genetics|February 11, 2014
Solving glycosylation disorders: fundamental approaches reveal complicated pathwaysHudson H Freeze, Jessica X Chong, Michael J Bamshad, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 27, 2013
Self-guided management of exome and whole-genome sequencing results: changing the results return modelJoon-Ho Yu, Seema M Jamal, Holly K Tabor, et al.American Journal of Medical Genetics. Part A|November 1, 2011
Genomics really gets personal: how exome and whole genome sequencing challenge the ethical framework of human genetics researchHolly K Tabor, Benjamin E Berkman, Sara Chandros Hull, et al.Developmental Medicine and Child Neurology|July 16, 2021
Mortality in pediatric hydrocephalusHannah M Tully, Dan Doherty, Mark WainwrightHandbook of Clinical Neurology|June 16, 2018
Genetics of cerebellar disordersEnza Maria Valente, Sara Nuovo, Dan DohertyNature Genetics|May 18, 2004
NIPBL, encoding a homolog of fungal Scc2-type sister chromatid cohesion proteins and fly Nipped-B, is mutated in Cornelia de Lange syndromeEmma T Tonkin, Tzu-Jou Wang, Steven Lisgo, et al.The Lancet. Neurology|March 23, 2013
Midbrain and hindbrain malformations: advances in clinical diagnosis, imaging, and geneticsDan Doherty, Kathleen J Millen, A James BarkovichAmerican Journal of Medical Genetics. Part A|April 24, 2013
Attitudes of African Americans toward return of results from exome and whole genome sequencingJoon-Ho Yu, Julia Crouch, Seema M Jamal, et al.Journal of Neurogenetics|March 27, 2013
Presence of epilepsy-associated variants in large exome databasesNatalya S Cherepanova, Elizabeth Leslie, Polly J Ferguson, et al.Pageof 36