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Clinical Genetics|February 22, 2023
Variants of LRP2, encoding a multifunctional cell-surface endocytic receptor, associated with hearing loss and retinal dystrophyRabia Faridi, Rizwan Yousaf, Shoujun Gu, et al.American Journal of Human Genetics|November 25, 2000
Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23J M Bork, L M Peters, S Riazuddin, et al.Frontiers in Nutrition|September 17, 2025
A multi-center, prospective, single-arm, open label, 13-month intervention study of a plant-based, high energy and protein enteral tube feed in home enterally tube fed patientsGary P Hubbard, Corbin Griffen, Rebecca Capener, et al.BMC Biology|February 6, 2025
Same data, different analysts: variation in effect sizes due to analytical decisions in ecology and evolutionary biologyElliot Gould, Hannah S Fraser, Timothy H Parker, et al.Pageof 68