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Clinica Chimica Acta; International Journal of Clinical Chemistry|November 28, 2008
Molecular analysis of Taiwanese patients with 3-hydroxy-3-methylglutaryl CoA lyase deficiencyWei-De Lin, Chung-Hsing Wang, Chien-Chen Lai, et al.
Biomedical Journal|January 18, 2022
Current understanding of the genetics of tourette syndromeWei-De Lin, Fuu-Jen Tsai, I-Ching Chou
Clinical Chemistry and Laboratory Medicine|February 27, 2010
FOXL2 mutations in Taiwanese patients with blepharophimosis, ptosis, epicanthus inversus syndromeWei-De Lin, I-Ching Chou, Ni-Chung Lee, et al.
Seizure|April 16, 2018
A novel PIGA mutation in a Taiwanese family with early-onset epileptic encephalopathyWei-De Lin, I-Ching Chou, Fuu-Jen Tsai, et al.
Biomedicine|December 19, 2014
Mutant EXT1 in Taiwanese Patients with Multiple Hereditary ExostosesWei-De Lin, Wuh-Liang Hwu, Chung-Hsing Wang, et al.
Biomedicine|November 20, 2016
A case of Pitt-Hopkins syndrome presented with Angelman-like syndromic phenotypesSyuan-Yu Hong, I-Ching Chou, Wei-De Lin, et al.
Biomedicine|November 16, 2022
Phenotype and genotype in a Taiwanese girl with Sotos SyndromeWei-De Lin, Chung-Hsing Wang, Fuu-Jen Tsai, et al.
Forensic Science, Medicine, and Pathology|February 12, 2024
Identification of the efficacy of parentage testing based on bi-allelic autosomal single nucleotide polymorphism markers in Taiwanese populationYu-Chia Chen, Wei-De Lin, Ting-Yuan Liu, et al.
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