Showing results (481-490 of 486) with videos related to
Sort By:
Pageof 49
You have reached the last page of results.This site can display upto 486 results.
Muscle & Nerve|September 6, 2016
Consecutive analysis of mutation spectrum in the dystrophin gene of 507 Korean boys with Duchenne/Becker muscular dystrophy in a single centerAnna Cho, Moon-Woo Seong, Byung Chan Lim, et al.Orphanet Journal of Rare Diseases|March 22, 2019
The Korean undiagnosed diseases program: lessons from a one-year pilot projectSoo Yeon Kim, Byung Chan Lim, Jin Sook Lee, et al.Journal of Pain Research|June 15, 2026
The Current Scope of Pain Medicine Fellowships: A Cross-Sectional Survey Study of Trainees, Directors, and Employers on Shaping Future LeadersUgur Yener, Scott G Pritzlaff, Micheal E Schatman, et al.Orphanet Journal of Rare Diseases|October 8, 2022
The Korean undiagnosed diseases program phase I: expansion of the nationwide network and the development of long-term infrastructureSoo Yeon Kim, Seungbok Lee, Hyewon Woo, et al.Human Molecular Genetics|January 20, 2026
SUPT16H-associated neurodevelopmental disorder and neurocristopathy: genetic and phenotypic spectrumEunhye Lee, Seungmin Sim, Hee-Jung Choi, et al.Nature Communications|January 8, 2024
Variants in the WDR44 WD40-repeat domain cause a spectrum of ciliopathy by impairing ciliogenesis initiationAndrea Accogli, Saurabh Shakya, Taewoo Yang, et al.Pageof 49