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胡務亮
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Showing results 24 to 41 of 41
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Issue Date
Title
Author(s)
Source
scopus
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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
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
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
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
2006
遺傳諮詢人員的介入對新生兒聽力篩檢陽性個案母親在知識、焦慮影響程度之探討
林毓婷; Lin, Yu-Ting
2005
高劑量tetrahydrobiopterin對發炎反應以及nitric oxide及自由基產生之影響
胡務亮