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Molecular Genetics and Metabolism|August 14, 2012
A role for inherited metabolic deficits in persistent developmental stutteringChangsoo Kang, Dennis DraynaAnnual Review of Genomics and Human Genetics|June 14, 2011
Genetics of speech and language disordersChangsoo Kang, Dennis DraynaJournal of Neurodevelopmental Disorders|August 19, 2011
Genetic approaches to understanding the causes of stutteringDennis Drayna, Changsoo KangJournal of Human Genetics|October 15, 2010
Characterization of a mutation commonly associated with persistent stuttering: evidence for a founder mutationAlison Fedyna, Dennis Drayna, Changsoo KangPlos One|December 18, 2015
A Genome-Wide Association Study Uncovers a Genetic Locus Associated with Thoracic-to-Hip Ratio in KoreansSeongwon Cha, Ah Yeon Park, Changsoo KangThe Journal of Biological Chemistry|September 30, 2011
Analysis of mannose 6-phosphate uncovering enzyme mutations associated with persistent stutteringWang-Sik Lee, Changsoo Kang, Dennis Drayna, et al.Genes & Genomics|March 9, 2021
Two missense mutations in GPNMB cause autosomal recessive amyloidosis cutis dyschromica in the consanguineous pakistani familiesObaid Ur Rahman, Jeena Kim, Caroline Mahon, et al.Genes & Genomics|June 24, 2018
Whole-exome sequencing analysis reveals co-segregation of a COL20A1 missense mutation in a Pakistani family with striate palmoplantar keratodermaMuhammad Ismail Khan, Soyeon Choi, Muhammad Zahid, et al.The New England Journal of Medicine|February 12, 2010
Mutations in the lysosomal enzyme-targeting pathway and persistent stutteringChangsoo Kang, Sheikh Riazuddin, Jennifer Mundorff, et al.JPMA. the Journal of the Pakistan Medical Association|February 27, 2019
Identification of Novel Mutation in CNGA3 gene by Whole-Exome Sequencing and In-Silico Analyses for Genotype-Phenotype Assessment with Autosomal Recessive Achromatopsia in Pakistani familiesMuhammad Waqar Arshad, Yujin Lee, Muhammad Arshad Malik, et al.Pageof 2