| Issue Date | Title | Author(s) | Source | scopus | WOS | Fulltext/Archive link |
| 2005 | KIF21A GENE C.2860C>T MUTATION IN CONGENITAL FIBROSIS OF EXTRAOCULAR MUSCLES TYPE 1 AND 3 | 林隆光; 簡穎秀; 鄔哲源; 王藹侯; 蔣書娟; 胡務亮 | MOLECULAR VISION | | | |
| 1993 | Measurement of Urinary Orotic Acid by Gas Chromatography-Mass Spectrometry | 胡務亮; Chou, S. P.; Wang, T. R.; Hwu, Wuh-Liang; Chou, S. P.; Wang, T. R. | Journal of Acta Paediatrica Sinica | | | |
| 2007 | Newborn Screening for Pompe Disease: Synthesis of the Evidence and Development of Screening Recommendations | Kemper, A. R.; Hwu, W.-L.; Lloyd-Puryear, M.; Kishnani, P. S.; 胡務亮 | PEDIATRICS | | | |
| 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; Tsai, W. Y.; Lee, J. S.; Wang, P. J.; Wang, T. R. | 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; Wang, T. R. | Journal of Acta Paediatrica Sinica | | | |
| 2005 | SIX NOVEL NPC1 MUTATIONS IN CHINESE PATIENTS WITH NIEMANN–PICK DISEASE TYPE C | 楊智超; 蘇怡寧; 余家利; 胡務亮; 李銘仁 | JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY | | | |
| 2007 | Tetrahydrobiopterin對於NO合 ’角局梇 (2/3) | 胡務亮 | | | |  |
| 2007 | Tetrahydrobiopterin對於NO合成 ﹞局梇 (3/3) | 胡務亮 | | | | |
| 1992 | Transfusion-Acquired Cytomegalovirus Infection in Children in a Hyperendemic Area | 李秉穎; 張美惠; 胡務亮; 高全良; 李慶雲; LEE, PING-ING; CHANG, MEI-HWEI; HWU, WUH-LIANG; KAO, CHUAN-LIANG; LEE, CHIN-YUN | JOURNAL OF MEDICAL | | | |
| 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; Hou, J. W.; Tsai, H. M. | Journal of Acta Paediatrica Sinica | | | |
| 1998 | 以抗體阻斷纖維芽細胞生長激素受體活化之研究 | 胡務亮 | | | | |
| 2009 | 原發性肉鹼缺乏症之新生兒篩檢個案的SLC22A5 (OCTN2)基因R254X突變分析 | 吳瓊娟; Wu, Chiung-Chuan | | | |  |
| 2009 | 唐氏症患者智能發展趨勢及語文與非語文能力分歧之探討 | 張麗滿; Chang, Lih-Maan | | | | |
| 2011 | 新生兒篩檢原發性肉鹼缺乏症R254X基因突變之研究 | 陳念宜; Chen, Nien-I | | | | |
| 2001 | 早老症分子機轉之研究 | 胡務亮 | | | | |
| 2008 | 羅素–西弗氏症與人類印記基因甲基化的定量與探討 | 錢薏蕾; Chien, I-Lei | | | | |
| 2007 | 羅素–西弗氏症與人類印記基因甲基化的關聯性研究 | 李美慧; Lee, Mei-Hui | | | | |
| 2008 | 臺灣遺傳檢驗與諮詢施行之現況分析與倫理反省 | 蔡甫昌; 張至寧; 楊智超; 胡務亮 | 醫學教育 | | | |
| 2005 | 親屬、友誼網絡對遺傳諮詢求醫行為之探討 | 郭惠珍; Kuo, Huey-Jen | | | | |
| 1996 | 遺傳疾病之對偶基因表現分析 | 胡務亮 | | | | |
