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The Journal of Clinical Investigation|March 27, 2012
Combining Cep290 and Mkks ciliopathy alleles in mice rescues sensory defects and restores ciliogenesisRivka A Rachel, Helen L May-Simera, Shobi Veleri, et al.
Annals of Internal Medicine|November 16, 2021
Comparative Effectiveness of an Automated Text Messaging Service for Monitoring COVID-19 at HomeM Kit Delgado, Anna U Morgan, David A Asch, et al.
American Journal of Surgery|September 19, 2017
A multi-institutional analysis of intraoperative radiotherapy for early breast cancer: Does age matter?A M Abbott, S A Valente, L Loftus, et al.
American Journal of Human Genetics|January 7, 2014
Mutations in TBC1D24, a gene associated with epilepsy, also cause nonsyndromic deafness DFNB86Atteeq U Rehman, Regie Lyn P Santos-Cortez, Robert J Morell, et al.
Journal of Alzheimer'S Disease Reports|October 22, 2025
Harnessing team science in dementia research: Insights from the Alzheimer's disease research group in South CarolinaSayema Akter, Eric Mishio Bawa, Nicholas Riccardi, et al.
Nature Genetics|October 28, 2008
Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humansZubair M Ahmed, Saber Masmoudi, Ersan Kalay, et al.
American Journal of Human Genetics|January 26, 2016
Autosomal-Recessive Hearing Impairment Due to Rare Missense Variants within S1PR2Regie Lyn P Santos-Cortez, Rabia Faridi, Atteeq U Rehman, et al.
Human Mutation|October 11, 2018
Global genetic insight contributed by consanguineous Pakistani families segregating hearing lossElodie M Richard, Regie Lyn P Santos-Cortez, Rabia Faridi, et al.
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