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Advances in Oto-Rhino-Laryngology|March 2, 2011
Basic medical genetics for the otolaryngologistRaye L Alford, Sandra A DarilekJournal of Neurovirology|September 17, 2004
Quantitative analysis of herpes simplex virus in cranial nerve gangliaJeffrey T Vrabec, Raye L AlfordCurrent Cardiology Reports|January 26, 2024
The Expansion of Genetic Testing in Cardiovascular Medicine: Preparing the Cardiology Community for the Changing LandscapeNosheen Reza, Raye L Alford, John W Belmont, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 13, 2012
Enhancing exposure to genetics and genomics through an innovative medical school curriculumShweta U Dhar, Raye L Alford, Elizabeth A Nelson, et al.BMC Medical Genetics|August 10, 2005
High frequency of the IVS2-2A>G DNA sequence variation in SLC26A5, encoding the cochlear motor protein prestin, precludes its involvement in hereditary hearing lossHsiao-Yuan Tang, Anping Xia, John S Oghalai, et al.American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|October 21, 2024
Family Lore, a Variant of Uncertain Significance, and CADASILRhys Duarte, Liesbeth Vossaert, Sandra A Darilek, et al.BMJ Open|May 21, 2015
DNA sequence analysis and genotype-phenotype assessment in 71 patients with syndromic hearing loss or auditory neuropathyHsiao-Yuan Tang, Ping Fang, Jerry W Lin, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 22, 2014
American College of Medical Genetics and Genomics guideline for the clinical evaluation and etiologic diagnosis of hearing lossRaye L Alford, Kathleen S Arnos, Michelle Fox, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 17, 2003
Early childhood hearing loss: clinical and molecular genetics. An educational slide set of the American College of Medical GeneticsRaye L Alford, Thomas B Friedman, Bronya J B Keats, et al.Pageof 2