Search Results - Wei De

Identification of a novel deletion mutation in PHKA2 in a taiwanese patient with type IXa glycogen storage disease by Wei-De Lin, Fuu-Jen Tsai, Chung-Hsing Wang

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Identification of one novel homozygous mutation in the NPR2 gene in a patient from Taiwan with acromesomelic dysplasia Maroteaux type by Wei-De Lin, Chung-Hsing Wang, Fuu-Jen Tsai

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Identification and Characterization of Mutations in the CLCN7 Gene in a Taiwanese Patient with Infantile Malignant Osteopetrosis by Wei-De Lin, Chung-Hsing Wang, Kang-His Wu, I-Ching Chou, Fuu-Jen Tsai

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Heterogeneous neurodevelopmental disorders in children with Kawasaki disease: what is new today? by Chien-Heng Lin, Wei-De Lin, I-Ching Chou, Inn-Chi Lee, Syuan-Yu Hong

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Stress hyperglycemia as first sign of asymptomatic type 1 diabetes: an instructive case by Wei-De Wang, Chun-Hao Chu, Chiung-Hsi Tien, Shuo-Yu Wang, Shih-Yao Liu, Chien-Ming Lin

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EZH2-Mediated Epigenetic Suppression of GDF15 Predicts a Poor Prognosis and Regulates Cell Proliferation in Non-Small-Cell Lung Cancer by Xiyi Lu, Xuezhi He, Jun Su, Jing Wang, Xinyin Liu, Kun Xu, Wei De, Erbao Zhang, Renhua Guo, Yuenian Eric Shi

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Infants of Mothers With Diabetes and Subsequent Attention Deficit Hyperactivity Disorder: A Retrospective Cohort Study by Chien-Heng Lin, Chien-Heng Lin, Wei-De Lin, I-Ching Chou, I-Ching Chou, Inn-Chi Lee, Syuan-Yu Hong

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Genetic Testing in Children with Developmental and Epileptic Encephalopathies: A Review of Advances in Epilepsy Genomics by Yu-Tzu Chang, Syuan-Yu Hong, Wei-De Lin, Chien-Heng Lin, Sheng-Shing Lin, Fuu-Jen Tsai, I-Ching Chou

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