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No Article Title /Author/Journal Title/Publication Year Cited
Long-Term Clinical Course of a Korean Patient with Chronic Neuropathic (type III) Gaucher Disease/
[Lee, Jun Hwa;] / Journal of Interdisciplinary Genomics / 2019    
0
Torticollis Management Using the Customized Soft Neck Collar in CATCH 22 Syndrome Combined with Klippel-Feil Anomaly: A Case Report/
[Moon, Myung-Hoon;Kim, Soo-Yeon;] / Journal of Interdisciplinary Genomics / 2019    
0
Genetic Therapies for Duchenne Muscular Dystrophy and Beyond/
[Shin, Jin-Hong;] / Journal of Interdisciplinary Genomics / 2019    
0
Novel variants of IDS gene, c.1224_1225insC, and recombinant variant of IDS gene, c.418+495_1006+1304del, in Two Families with Mucopolysaccharidosis type II/
[Cheon, Chong Kun;] / Journal of Interdisciplinary Genomics / 2019    
0
First Korean Case of 16p11.2 Duplication Syndrome Diagnosed by Chromosomal Microarray Analysis/
[Shim, Ye Jee;Park, So Yun;Jung, Nani;Kang, Seok Jin;Kim, Heung Sik;Ha, Jung-Sook;] / Journal of Interdisciplinary Genomics / 2019    
0
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