Application of Whole Exome Sequencing and Functional Annotations to Identify Genetic Variants Associated with Marfan Syndrome

por Lin, Min-Rou, Chang, Che-Mai, Ting, Jafit, Chang, Jan-Gowth, Chou, Wan-Hsuan, Huang, Kuei-Jung, Cheng, Gloria, Chang, Hsiao-Huang, Chang, Wei-Chiao
Publicado 2022

Whole-Exome Sequencing Identifies Genetic Variants for Severe Adolescent Idiopathic Scoliosis in a Taiwanese Population

por Lin, Min-Rou, Chou, Po-Hsin, Huang, Kuei-Jung, Ting, Jafit, Liu, Chia-Ying, Chou, Wan-Hsuan, Lin, Gan-Hong, Chang, Jan-Gowth, Ikegawa, Shiro, Wang, Shih-Tien, Chang, Wei-Chiao
Publicado 2022