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 | | | |
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 | | | |
2011 | Citrin缺乏症在新生兒篩檢的基因突變研究 | 王里勻; Wang, Li-Yun | | | | |
1991 | A Clinical Observation in Achondroplasia | 胡務亮; Wang, T. R.; Hwu, Wuh-Liang | Journal of Acta Paediatrica Sinica | | | |
1991 | A Clinical Study in Intravenous Immunoglobulin Therapy for Childhood Idiopathic Chromobocytopenic Purpura | Lin, D. T.; 胡務亮; Lin, K. H.; Lin, K. S.; Hwu, Wuh-Liang | Journal of the Formosan Medical Association | | | |
1991 | COLOCALIZATION IN PERICENTRAL HEPATOCYTES IN ADULT MICE AND SIMILARITY IN DEVELOPMENTAL EXPRESSION PATTERN OF ORNITHINE AMINOTRANSFERASE AND GLUTAMINE SYNTHETASE IN mRNA | 顧泉; 胡務亮; KUO, FRANK C; HWU, WUH-LIANG; VALLE D | PROCEEDINGS OF THE | | | |
1991 | Colocalization in Pericentral Hepatocytes in Adult Mice and Similarity in Developmental Expression Pattern of Ornithine Aminotransferase and Glutamine Synthetase mRNA | Kuo, F. C.; 胡務亮; Valle, D.; Darnell, J. E.; Hwu, Wuh-Liang | Proceedings of the National Academy of Sciences of the United States of America | | | |
1989 | Current Status of Detecting Fragible-X Syndrome Using Molecular Biology Techniques at the National Taiwan University Hospital | Wang, Tso-Ren; Hwu, Wuh-Liang; 胡務亮 | 1992 San Diego Conference on Nucleic Acids:Genetic Recognition | | | |
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 | Diagnosis of I-Cell Disease | 胡務亮; 蔣書娟; 王文娟; 王作仁; HWU, WUH-LIANG; CHIANG, SHU-CHUAN; WANG, WEN-CHUAN; WANG, TSO-REN | 中華民國小兒科醫學會雜誌,v.35 | | | |
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 | | | |
1992 | DNA Fingerprinting in the Chinese with an Oligonucleotide Probe (GTG) | 林凱信; 陳榮隆; Wang, Tso-Renmin; Su, Ih-Jen; Lin, Kuo-Sin; 胡務亮; Hwu, Wuh-Liang | Journal of the Formosan Medical Association | | | |
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 | | | |
2001 | GTP CYCLOHYDROLASE I 基因轉殖小鼠啟動子表現及表現型分析 | 胡務亮 | | | | |
2002 | GTP Cyclohydrolase I 突變及Splicing之分子結構機轉(1/3) | 胡務亮 | | | | |
2003 | GTP Cyclohydrolase I 突變及Splicing之分子結構機轉(2/3) | 胡務亮 | | | | |
2004 | GTP Cyclohydrolase I 突變及Splicing之分子結構機轉(3/3) | 胡務亮 | Biochemical and Biophysical Research Communications (306),937–942 | | | |
1989 | Hereditary Progressive Dystonia with Marked Diurnal Fluctuation:Report of A Case | 王本榮; Shen, Y. Z.; 胡務亮; Wang, Pen-Jung; Hwu, Wuh-Liang | Journal of Acta Paediatrica Sinica | | | |
1989 | Hereditary Progrressive Dystonia with Marked Diurnal Fluctuation, Report of a Case | 胡務亮; Wang, P. J.; Shen, Y. Z.; Hwu, Wuh-Liang | Journal of Acta Paediatrica Sinica | | | |