Showing results (391-400 of 467) with videos related to

Sort By:
Pageof 47
The Journal of Clinical Investigation|February 9, 2016
FOXE3 mutations predispose to thoracic aortic aneurysms and dissectionsShao-Qing Kuang, Olga Medina-Martinez, Dong-Chuan Guo, et al.
Neurology|March 14, 2014
GABRA1 and STXBP1: novel genetic causes of Dravet syndromeGemma L Carvill, Sarah Weckhuysen, Jacinta M McMahon, 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.
American Journal of Human Genetics|December 24, 2013
Mutations in CSPP1 cause primary cilia abnormalities and Joubert syndrome with or without Jeune asphyxiating thoracic dystrophyKarina Tuz, Ruxandra Bachmann-Gagescu, Diana R O'Day, et al.
Nature Communications|May 16, 2024
Impacts of human mobility on the citywide transmission dynamics of 18 respiratory viruses in pre- and post-COVID-19 pandemic yearsAmanda C Perofsky, Chelsea L Hansen, Roy Burstein, et al.
American Journal of Human Genetics|April 2, 2013
Mutations in KCTD1 cause scalp-ear-nipple syndromeAlexander G Marneros, Anita E Beck, Emily H Turner, et al.
Biorxiv : the Preprint Server for Biology|March 30, 2023
Modulation of FGF pathway signaling and vascular differentiation using designed oligomeric assembliesNatasha I Edman, Rachel L Redler, Ashish Phal, et al.
Pageof 47