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Journal of the American Chemical Society|February 16, 2026
Lithium and Sodium Intercalation with Multielectron Redox in Vacancy Ordered and Vacancy Disordered Cation-Deficient Anti-NASICON Niobium(V) PhosphatesJui-Cheng Hsiao, Caroline Hou, Tianren Zhang, et al.
Human Molecular Genetics|October 24, 2002
Mutation of a transcription factor, TFCP2L3, causes progressive autosomal dominant hearing loss, DFNA28Linda M Peters, David W Anderson, Andrew J Griffith, et al.
American Journal of Medical Genetics. Part A|September 10, 2005
Stickler syndrome: clinical characteristics and diagnostic criteriaPeter S Rose, Howard P Levy, Ruth M Liberfarb, et al.
Journal of the Association for Research in Otolaryngology : JARO|October 17, 2002
Knock-in mouse model for resistance to thyroid hormone (RTH): an RTH mutation in the thyroid hormone receptor beta gene disrupts cochlear morphogenesisAndrew J Griffith, Yvonne M Szymko, Masahiro Kaneshige, et al.
Clinical Genetics|February 19, 2008
A locus for autosomal dominant progressive non-syndromic hearing loss, DFNA27, is on chromosome 4q12-13.1L M Peters, R A Fridell, E T Boger, et al.
Ultramicroscopy|November 14, 2021
Atom probe specimen preparation methods for nanoparticlesJiangtao Qu, Wenjie Yang, Tianhao Wu, et al.
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