Issue Date | Title | Author(s) | Source | scopus | WOS | Fulltext/Archive link |
1989 | Alkaptonuria in a Chinese Baby Case Report | Wang, T. R.; 胡務亮; Hwu, Wuh-Liang | Journal of Inherited Metabolic Disease | | | |
1991 | The Analysis of Plain Film Presentation and Bone Age of Achondroplasia | Lin, S. C.; 李瑤華; Wang, T. R.; Li, Yiu-Wah | Chang Gung Medical Journal | | | |
1990 | Apert Syndrome Associated with Septo-Optic Dysplasia | 沈友仁; 滕儒錚; 王本榮; Wang, T. R.; Shen, Y. Z.; Wang, Pen-Jung | Pediatric Neurology | | | |
1993 | Atlantoaxial Subluxation and Syringomyelia in Down Syndrome | 王本榮; Hou, J. W.; Lin, Y. J.; Wang, T. R.; Wang, Pen-Jung | Journal of Acta Paediatrica Sinica | | | |
1996 | Camptomelic dysplasia: report of one case | PO-NIEN TSAO ; Teng, R. J.; WUH-LIANG HWU ; Tsou Yau, K. I.; Wang, T. R. | Zhonghua Minguo xiao er ke yi xue hui za zhi [Journal]. Zhonghua Mingu o xiao er ke yi xue hui | | | |
1994 | Case Report:Fucosidosis in a Chinese Girl | 胡務亮; Chuang, S. C.; Wang, W. C.; Wang, T. R.; Hwu, Wuh-Liang | Journal of Inherited Metabolic Disease | | | |
1991 | A Clinical Observation in Achondroplasia | 胡務亮; Wang, T. R.; Hwu, Wuh-Liang | Journal of Acta Paediatrica Sinica | | | |
1994 | Congenital Nephrotic Syndrome with Microcephaly:Report of A Case | 王本榮; Yu, C. H.; 蔡文雄; 曹永魁; Wang, T. R.; Tsau, Yong-Kwei | Journal of the Formosan Medical Association | | | |
1995 | Cytogenetic Study of Mentally Retarded Children in Taipei | Sheng, W. W.; Lai, Y. M.; 胡務亮; Wang, T. R.; Wuu, K. I.; Hwu, Wuh-Liang | Biomedical Science | | | |
1994 | The Diagnosis of I-Cell Disease | 胡務亮; Chuang, S. C.; Wang, W. C.; Wang, T. R.; Hwu, Wuh-Liang | Journal of Acta Paediatrica Sinica | | | |
1993 | Fragile X Mental Retardation:A Combination of Cytogenetic and Molecular Approaches with More Stress on DNA Analysis | Wang, T. R.; 胡務亮; Hou, J. W.; Chou, S. P.; Liu, C. H.; Hwu, Wuh-Liang | Journal of Acta Paediatrica Sinica | | | |
1995 | Glucose-6-phosphate Gene G327 is a Common Mutation in Chinese Patients with Glycogen Storage Disease Type I | 胡務亮; Wang, W. C.; Cheng, J. R.; Chuang, S. C.; Tsai, L. P.; Wang, T. R.; Hwu, Wuh-Liang | Human Molecular Genetics | | | |
1989 | Human Sperm CVhrosome Analysis in Primary Infertility:A Prelimimary Report | Hsu, C. C.; Lien, Y. R.; Yang, Yu-Shih; Chuang, S. M.; Lee, Tzu-Yao; Lin, S. J.; 楊友仕; Wang, T. R.; 李鎡堯 | Journal of the Formosan Medical Association | | | |
1993 | In Vitro DNA Methylation Inhibits FMR-1 Promoter | 胡務亮; Lee, Y. M.; Lee, S. C.; Wang, T. R.; Hwu, Wuh-Liang | Biochemical and Biophysical Research Communications | | | |
1993 | Measurement of Urinary Orotic Acid by Gas Chromatography-Mass Spectrometry | 胡務亮; Chou, S. P.; Wang, T. R.; Hwu, Wuh-Liang | Journal of Acta Paediatrica Sinica | | | |
1989 | Metachromatic Leukodystrophy:Four Cases Report | 王本榮; Wang, T. R.; Shen, Y. Z.; Lee, C. Y.; Wang, Pen-Jung | Journal of Acta Paediatrica Sinica | | | |
1992 | Prader-Willi Syndrome with Chromosome 15 Intersitital Deletion:Report of a Case | 胡務亮; Tsai, W. Y.; Lee, J. S.; Wang, P. J.; Wang, T. R.; Hwu, Wuh-Liang | Journal of Acta Paediatrica Sinica | | | |
1991 | Quantification of Arylsulfatase B Activity and the Diagnosis of Maroteaux-Lamy Syndrome | 胡務亮; Wang, T. R.; Hwu, Wuh-Liang | Journal of Acta Paediatrica Sinica | | | |
1996 | Sex determination in infants with ambiguous genitalia using the polymerase chain reaction of an X-Y homologous region | Tsai, C. H.; Tsai, F. J.; WUH-LIANG HWU ; Wang, T. R.; Shu, S. G.; Liu, S. C. | Zhonghua Minguo xiao er ke yi xue hui za zhi [Journal]. Zhonghua Mingu o xiao er ke yi xue hui | | | |
1994 | Y-Specific Polymerase Chain Reaction for the Interpretation of Chromosome Marker | Wang, T. R.; 胡務亮; Hou, J. W.; Tsai, H. M.; Liu, C. H.; Hwu, Wuh-Liang | Journal of Acta Paediatrica Sinica | | | |