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Institution	Date	Title	Author
臺大學術典藏	2020-03-06T08:25:45Z	Hepatoblastoma in an infant with Beckwith-Wiedemann Syndrome.	Tsai S.Y.;Yung-Ming Jeng;Hwu W.L.;Ni Y.H.;Chang M.H.;Wang T.R.; Tsai S.Y.; YUNG-MING JENG; Hwu W.L.; Ni Y.H.; Chang M.H.; Wang T.R.
臺大學術典藏	2020-03-05T01:18:02Z	Neuronal firing patterns outweigh circuitry oscillations in parkinsonian motor control	Pan M.-K.; Kuo S.-H.; CHUN-HWEI TAI; Liou J.-Y.; Pei J.-C.; Chang C.-Y.; Wang Y.-M.; Liu W.-C.; Wang T.-R.; Lai W.-S.; Kuo C.-C.
臺大學術典藏	2020-03-02T03:11:31Z	Kleine-Levin syndrome in a boy with Prader-Willi syndrome	Susan Shur-Fen Gau;Soong W.-T.;Liu H.-M.;Hou J.-W.;Tsai W.-Y.;Chiu Y.-N.;Yeh Y.-C.;Wang P.-J.;Wang T.-R.; SUSAN SHUR-FEN GAU; Soong W.-T.; Liu H.-M.; Hou J.-W.; Tsai W.-Y.; Chiu Y.-N.; Yeh Y.-C.; Wang P.-J.; Wang T.-R.
臺大學術典藏	2020-02-19T01:36:03Z	Human sperm chromosome analysis in primary infertility: a preliminary report.	Lin S.J;Hsu C.C;Yih-Ron Lien;Yang Y.S;Wang T.R;Chuang S.M;Lee T.Y.; Lin S.J; Hsu C.C; YIH-RON LIEN; Yang Y.S; Wang T.R; Chuang S.M; Lee T.Y.
臺大學術典藏	2020-02-17T08:07:45Z	Human sperm chromosome analysis in primary infertility: a preliminary report.	Lin S.J; Hsu C.C; Lien Y.R; YU-SHIH YANG; Wang T.R; Chuang S.M; Lee T.Y.
臺大學術典藏	2020-02-03T08:15:30Z	Maternal and fetal outcome of pregnant women with idiopathic thrombocytopenic purpura: retrospective analysis of 25 pregnancies.	Hsiao-Lin Hwa;Chen R.J.;Chen Y.C.;Wang T.R.;Huang S.C.;Chow S.N.; HSIAO-LIN HWA; Chen R.J.; Chen Y.C.; Wang T.R.; Huang S.C.; Chow S.N.
臺大學術典藏	2020-02-03T08:15:25Z	Erratum: Molecular genetic study of Pompe disease in Chinese patients in Taiwan (Human Mutation (1999) 13 (380-384))	Ko T.-M.;Hwu W.-L.;Lin Y.-W.;Tseng L.-H.;Hsiao-Lin Hwa;Wang T.-R.;Chuang S.- M.;Hayashi K.; Ko T.-M.; Hwu W.-L.; Lin Y.-W.; Tseng L.-H.; HSIAO-LIN HWA; Wang T.-R.; Chuang S.- M.; Hayashi K.
臺大學術典藏	2020-02-03T08:15:24Z	Molecular genetic study of Pompe disease in Chinese patients in Taiwan	Ko T.-M.; Hwu W.-L.; Lin Y.-W.; Tseng L.-H.; HSIAO-LIN HWA; Wang T.-R.; Chuang S.-M.; Ko T.-M.;Hwu W.-L.;Lin Y.-W.;Tseng L.-H.;Hsiao-Lin Hwa;Wang T.-R.;Chuang S.-M.
臺大學術典藏	2018-09-10T07:33:03Z	Corneal opacity and congenital glaucoma associated with massive heparan sulfaturia: Report of one case	Lin, S.-C.;Hu, F.-R.;Hou, J.-W.;Yao, Y.-T.;Wang, T.-R.;Hung, P.-T.; FUNG-RONG HU
臺大學術典藏	2018-09-10T07:24:56Z	Molecular genetic study of Pompe disease in Chinese patients in Taiwan	Ko, T.-M.;Hwu, W.-L.;Lin, Y.-W.;Tseng, L.-H.;Hwa, H.-L.;Wang, T.-R.;Chuang, S.-M.; LI-HUI TSENG; HSIAO-LIN HWA
臺大學術典藏	2018-09-10T07:24:56Z	Erratum: Molecular genetic study of Pompe disease in Chinese patients in Taiwan (Human Mutation (1999) 13 (380-384))	Ko, T.-M.;Hwu, W.-L.;Lin, Y.-W.;Tseng, L.-H.;Hwa, H.-L.;Wang, T.-R.;Chuang S.-, M.;Hayashi, K.; LI-HUI TSENG; HSIAO-LIN HWA
臺大學術典藏	2018-09-10T07:22:20Z	Detection of KAL-1 gene deletion with fluorescence in situ hybridization	Hou, J.-W.;Tsai, W.-Y.;Wang, T.-R.; WEN-YU TSAI
臺大學術典藏	2018-09-10T06:14:53Z	CATCH 22: Deletion of locus 22Q11 in velocardiofacial syndrome, digeorge anomaly, and nonsyndromic conotruncal defects	Hou, J.-W.;Wang, J.-K.;Tsai, W.-Y.;Chou, C.-C.;Wang, T.-R.; WEN-YU TSAI
臺大學術典藏	2018-09-10T06:14:53Z	Partial DiGeorge anomaly associated with 10p deletion	Hsu, H.-L.;Hsiao, P.-H.;Hou, J.-W.;Tsai, W.-Y.;Wang, T.-R.; WEN-YU TSAI
臺大學術典藏	2018-09-10T06:06:32Z	Oculomotor apraxia in a case of Gaucher's disease with homozygous T1448C mutation.	Tsai, L.P.;Sue, W.C.;Hwu, W.L.;Lin, K.H.;Wang, T.R.; KAI-HSIN LIN
臺大學術典藏	2018-09-10T05:46:39Z	Kleine-Levin syndrome in a boy with Prader-Willi syndrome	Gau, S.-F.;Soong, W.-T.;Liu, H.-M.;Hou, J.-W.;Tsai, W.-Y.;Chiu, Y.-N.;Yeh, Y.-C.;Wang, P.-J.;Wang, T.-R.; WEN-YU TSAI
臺大學術典藏	2018-09-10T05:46:28Z	Camptomelic dysplasia: report of one case.	Tsao, P.N.;Teng, R.J.;Hwu, W.L.;Tsou Yau, K.I.;Wang, T.R.; PO-NIEN TSAO
臺大學術典藏	2018-09-10T05:12:25Z	Prevalence of permanent primary congenital hypothyroidism in Taiwan.	Tsai, W.Y.;Lee, J.S.;Chao, M.C.;Chen, L.Y.;Lin, S.J.;Wu, K.H.;Wang, T.R.;Chen, J.S.;Chuang, S.M.; WEN-YU TSAI
臺大學術典藏	2018-09-10T04:43:31Z	Congenital nephrotic syndrome with microcephaly: report of a case.	Yu, C.H.;Tsai, W.S.;Wang, P.J.;Tsau, Y.K.;Tseng, G.C.;Wang, T.R.; YONG-KWEI TSAU
臺大學術典藏	2018-09-10T04:17:49Z	DNA fingerprinting in the Chinese with an oligonucleotide probe (GTG)5.	Hwu, W.L.;Chen, R.L.;Lin, K.H.;Wang, T.R.; KAI-HSIN LIN
臺大學術典藏	2018-09-10T04:05:38Z	Familial nephrogenic diabetes insipidus: report of two families.	Lee, J.S.;Tsai, W.Y.;Tsai, W.S.;Tsau, Y.K.;Chen, C.H.;Wang, T.R.; WEN-YU TSAI
臺大學術典藏	2018-09-10T04:05:21Z	Familial nephrogenic diabetes insipidus: report of two families.	Lee, J.S.;Tsai, W.Y.;Tsai, W.S.;Tsau, Y.K.;Chen, C.H.;Wang, T.R.; YONG-KWEI TSAU
臺大學術典藏	2018-09-10T03:41:51Z	Prader-Willi syndrome with chromosome 15 interstitial deletion: report of one case.	Hwu, W.L.;Tsai, W.Y.;Lee, J.S.;Wang, P.J.;Wang, T.R.; WEN-YU TSAI
臺大學術典藏	2018-09-10T03:32:25Z	Wilson disease presenting as fulminant hepatic failure, acute hemolytic anemia and renal failure: report of one case	Tseng, C.L.;Tsai, S.L.;Lin, K.H.;Chang, M.H.;Wang, T.R.;Hsu, Y.H.;Hsu, H.C.; KAI-HSIN LIN
臺大學術典藏	2018-09-10T03:24:11Z	Wiedemann-Beckwith syndrome with congenital central hypothyroidism in one of monozygotic twins.	Chien, C.H.;Lee, J.S.;Tsai, W.Y.;Wang, T.R.; WEN-YU TSAI
臺大學術典藏	1999	Molecular genetic study of Pompe disease in Chinese patients in Taiwan	Ko T.-M.;Wuh-Liang Hwu;Lin Y.-W.;Tseng L.-H.;Hwa H.-L.;Wang T.-R.;Chuang S.-M.; Ko T.-M.; WUH-LIANG HWU; Lin Y.-W.; Tseng L.-H.; Hwa H.-L.; Wang T.-R.; Chuang S.-M.
國立成功大學	1998-06	A curvature-ovalization measurement apparatus for circular tubes under cyclic bending	Pan, Wen-Fung; Wang, T. R.; Hsu, C. M.
臺大學術典藏	1998	Recommendations for management of severe enterovirus infection in Taiwan	PING-ING LEE; Lee C.-Y.; Wang T.-R.
臺大學術典藏	1996	Oculomotor apraxia in a case of Gaucher's disease with homozygous T1448C mutation.	Tsai L.P.;Sue W.C.;Wuh-Liang Hwu;Lin K.H.;Wang T.R.; Tsai L.P.; Sue W.C.; WUH-LIANG HWU; Lin K.H.; Wang T.R.
臺大學術典藏	1996	Hepatoblastoma in an infant with Beckwith-Wiedemann Syndrome.	Wang T.R.; Chang M.H.; YEN-HSUAN NI; Hwu W.L.; Jeng Y.M.; Tsai S.Y.;Jeng Y.M.;Hwu W.L.;Yen-Hsuan Ni;Chang M.H.;Wang T.R.; Tsai S.Y.
國立臺灣大學	1995	Cytogenetic Study of Mentally Retarded Children in Taipei	Sheng, W. W.; Lai, Y. M.; 胡務亮; Wang, T. R.; Wuu, K. I.; Sheng, W. W.; Lai, Y. M.; Hwu, Wuh-Liang; Wang, T. R.; Wuu, K. I.
國立臺灣大學	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; Wang, W. C.; Cheng, J. R.; Chuang, S. C.; Tsai, L. P.; Wang, T. R.
國立臺灣大學	1994	Case Report:Fucosidosis in a Chinese Girl	胡務亮; Chuang, S. C.; Wang, W. C.; Wang, T. R.; Hwu, Wuh-Liang; Chuang, S. C.; Wang, W. C.; Wang, T. R.
國立臺灣大學	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.; 王本榮; Yu, C. H.; 蔡文雄; Tsau, Yong-Kwei; Wang, T. R.
國立臺灣大學	1994	The Diagnosis of I-Cell Disease	胡務亮; Chuang, S. C.; Wang, W. C.; Wang, T. R.; Hwu, Wuh-Liang; Chuang, S. C.; Wang, W. C.; Wang, T. R.
國立臺灣大學	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.; Wang, T. R.; Hwu, Wuh-Liang; Hou, J. W.; Tsai, H. M.; Liu, C. H.
國立臺灣大學	1993	Atlantoaxial Subluxation and Syringomyelia in Down Syndrome	王本榮; Hou, J. W.; Lin, Y. J.; Wang, T. R.; Wang, Pen-Jung; Hou, J. W.; Lin, Y. J.; Wang, T. R.
國立臺灣大學	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.; Wang, T. R.; Hwu, Wuh-Liang; Hou, J. W.; Chou, S. P.; Liu, C. H.
國立臺灣大學	1993	In Vitro DNA Methylation Inhibits FMR-1 Promoter	胡務亮; Lee, Y. M.; Lee, S. C.; Wang, T. R.; Hwu, Wuh-Liang; Lee, Y. M.; Lee, S. C.; Wang, T. R.
國立臺灣大學	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.
國立臺灣大學	1992	Familial Nephrogenic Diabetes Insipidus:Report of Two Families	曹永魁; Lee, J. S.; Tsai, W. Y.; 蔡文雄; Chen, C. H.; Wang, T. R.; Tsau, Yong-Kwei; Lee, J. S.; Tsai, W. Y.; Tsai, Wen-Shiung; Chen, C. H.; Wang, T. R.
國立臺灣大學	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.
國立臺灣大學	1992	Crisis in Gaucher Disease Simulating Osteomyelitis:Report of One Case	Lai, Y. C.; Wang, T. R.; 謝貴雄; Lee, C. Y.; Li, Y. W.; Lai, Y. C.; Wang, T. R.; Hsieh, Kue-Hsiung; Lee, C. Y.; Li, Y. W.
國立臺灣大學	1991	A Clinical Observation in Achondroplasia	胡務亮; Wang, T. R.; Hwu, Wuh-Liang; Wang, T. R.
國立臺灣大學	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.
國立臺灣大學	1991	The Analysis of Plain Film Presentation and Bone Age of Achondroplasia	Lin, S. C.; 李瑤華; Wang, T. R.; Lin, S. C.; Li, Yiu-Wah; Wang, T. R.
國立臺灣大學	1990	Apert Syndrome Associated with Septo-Optic Dysplasia	沈友仁; 滕儒錚; 王本榮; Wang, T. R.; Shen, Y. Z.; 沈友仁; 滕儒錚; Wang, Pen-Jung; Wang, T. R.; Shen, Y. Z.
國立臺灣大學	1989	Alkaptonuria in a Chinese Baby Case Report	Wang, T. R.; 胡務亮; Wang, T. R.; Hwu, Wuh-Liang
國立臺灣大學	1989	Metachromatic Leukodystrophy:Four Cases Report	王本榮; Wang, T. R.; Shen, Y. Z.; Lee, C. Y.; Wang, Pen-Jung; Wang, T. R.; Shen, Y. Z.; Lee, C. Y.
國立臺灣大學	1989	Human Sperm CVhrosome Analysis in Primary Infertility:A Prelimimary Report	Lin, S. J.; Hsu, C. C.; Lien, Y. R.; 楊友仕; Wang, T. R.; Chuang, S. M.; 李鎡堯; Lin, S. J.; Hsu, C. C.; Lien, Y. R.; Yang, Yu-Shih; Wang, T. R.; Chuang, S. M.; Lee, Tzu-Yao

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