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Acta Paediatrica Taiwanica = Taiwan Er Ke Yi Xue Hui Za Zhi|July 27, 2000
Molecular diagnosis of Apert syndrome in Chinese patientsF J Tsai, C H Tsai, C T Peng, et al.
Journal of Endocrinological Investigation|May 25, 2024
Impact of polygenic risk score for triglyceride trajectory and diabetic complications in subjects with type 2 diabetes based on large electronic medical record data from Taiwan: a case control studyW-L Liao, Y-C Huang, Y-W Chang, et al.
Acta Paediatrica Taiwanica = Taiwan Er Ke Yi Xue Hui Za Zhi|July 27, 2000
An R248C mutation of FGFR3 leading to thanatophoric dysplasia type IF J Tsai, L P Tsai, S P Lin, et al.
Prenatal Diagnosis|July 17, 1998
Prenatal diagnosis of Apert syndromeC C Chang, F J Tsai, H D Tsai, et al.
Cytogenetic and Genome Research|February 7, 2008
Identification and characterization of a new type of asymmetrical dicentric chromosome derived from a single maternal chromosome 18C C Lin, Y-C Li, P-P Liu, et al.
International Journal of Obesity (2005)|September 21, 2011
Gene polymorphisms of adiponectin and leptin receptor are associated with early onset of type 2 diabetes mellitus in the Taiwanese populationW-L Liao, C-C Chen, C-T Chang, et al.
International Journal of Immunogenetics|July 13, 2010
Association of COL11A2 polymorphism with susceptibility to Kawasaki disease and development of coronary artery lesionsJ J Sheu, Y J Lin, J S Chang, et al.
Journal of Biological Regulators and Homeostatic Agents|July 9, 2013
Genetic variability in copper-transporting P-type adenosine triphosphatase (ATP7B) is associated with Alzheimer's disease in a Chinese populationH P Liu, W Y Lin, W F Wang, et al.
Human Mutation|November 26, 1998
Mutation analysis of Wilson disease in Taiwan and description of six new mutationsC H Tsai, F J Tsai, J Y Wu, et al.
Journal of Biological Regulators and Homeostatic Agents|October 5, 2012
Association analysis of dopaminergic gene variants (Comt, Drd4 And Dat1) with Alzheimer s diseaseW Y Lin, B T Wu, C C Lee, et al.
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