| 臺大學術典藏 |
2020-12-24T06:16:18Z |
Primary coenzyme Q10 deficiency-7: expanded phenotypic spectrum and a founder mutation in southern Chinese
|
Fung J.L.-F.; Yeung K.-S.; Mak C.C.-Y.; Smeitink J.; Rodenburg R.J.T.; Chong S.-C.; Tsoi C.; Chan V.C.-M.; Kuo P.-L.; Hwu W.-L.; YIN-HSIU CHIEN; Quinzii C.M.; Lin S.-P.; Chou Y.-Y.; Kwong A.K.-Y.; Willis B.; Tse D.M.L.; Yu M.H.-C.; Tsang M.H.-Y.; Lai S.; Ho M.S.-P.; Lam W.; Hui J.; Lee N.-C.; Fung C.-W.; Chung B.H.-Y. |
| 臺大學術典藏 |
2020-12-16T02:25:03Z |
Primary coenzyme Q10 deficiency-7: expanded phenotypic spectrum and a founder mutation in southern Chinese
|
Yu M.H.-C.;Tsang M.H.-Y.;Lai S.;Ho M.S.-P.;Tse D.M.L.;Willis B.;Kwong A.K.-Y.;Chou Y.-Y.;Lin S.-P.;Quinzii C.M.;Wuh-Liang Hwu;Chien Y.-H.;Kuo P.-L.;Chan V.C.-M.;Tsoi C.;Chong S.-C.;Rodenburg R.J.T.;Smeitink J.;Mak C.C.-Y.;Yeung K.-S.;Fung J.L.-F.;Lam W.;Hui J.;Lee N.-C.;Fung C.-W.;Chung B.H.-Y.; Yu M.H.-C.; Tsang M.H.-Y.; Lai S.; Ho M.S.-P.; Tse D.M.L.; Willis B.; Kwong A.K.-Y.; Chou Y.-Y.; Lin S.-P.; Quinzii C.M.; WUH-LIANG HWU; Chien Y.-H.; Kuo P.-L.; Chan V.C.-M.; Tsoi C.; Chong S.-C.; Rodenburg R.J.T.; Smeitink J.; Mak C.C.-Y.; Yeung K.-S.; Fung J.L.-F.; Lam W.; Hui J.; Lee N.-C.; Fung C.-W.; Chung B.H.-Y. |
| 臺大學術典藏 |
2020-12-16T02:25:03Z |
Primary coenzyme Q10 deficiency-7: expanded phenotypic spectrum and a founder mutation in southern Chinese
|
Yu M.H.-C.;Tsang M.H.-Y.;Lai S.;Ho M.S.-P.;Tse D.M.L.;Willis B.;Kwong A.K.-Y.;Chou Y.-Y.;Lin S.-P.;Quinzii C.M.;Wuh-Liang Hwu;Chien Y.-H.;Kuo P.-L.;Chan V.C.-M.;Tsoi C.;Chong S.-C.;Rodenburg R.J.T.;Smeitink J.;Mak C.C.-Y.;Yeung K.-S.;Fung J.L.-F.;Lam W.;Hui J.;Lee N.-C.;Fung C.-W.;Chung B.H.-Y.; Yu M.H.-C.; Tsang M.H.-Y.; Lai S.; Ho M.S.-P.; Tse D.M.L.; Willis B.; Kwong A.K.-Y.; Chou Y.-Y.; Lin S.-P.; Quinzii C.M.; WUH-LIANG HWU; Chien Y.-H.; Kuo P.-L.; Chan V.C.-M.; Tsoi C.; Chong S.-C.; Rodenburg R.J.T.; Smeitink J.; Mak C.C.-Y.; Yeung K.-S.; Fung J.L.-F.; Lam W.; Hui J.; Lee N.-C.; Fung C.-W.; Chung B.H.-Y. |
| 臺大學術典藏 |
2020-12-09T01:38:15Z |
Exome sequencing for paediatric-onset diseases: impact of the extensive involvement of medical geneticists in the diagnostic odyssey
|
Mak C.C.;Leung G.K.;Mok G.T.;Yeung K.S.;Yang W.;Fung C.-W.;Chan S.H.;Lee S.-L.;Ni-Chung Lee;Pfundt R.;Lau Y.-L.;Chung B.H.; Mak C.C.; Leung G.K.; Mok G.T.; Yeung K.S.; Yang W.; Fung C.-W.; Chan S.H.; Lee S.-L.; NI-CHUNG LEE; Pfundt R.; Lau Y.-L.; Chung B.H. |
| 臺大學術典藏 |
2020-12-09T01:38:15Z |
Exome sequencing for paediatric-onset diseases: impact of the extensive involvement of medical geneticists in the diagnostic odyssey
|
Mak C.C.;Leung G.K.;Mok G.T.;Yeung K.S.;Yang W.;Fung C.-W.;Chan S.H.;Lee S.-L.;Ni-Chung Lee;Pfundt R.;Lau Y.-L.;Chung B.H.; Mak C.C.; Leung G.K.; Mok G.T.; Yeung K.S.; Yang W.; Fung C.-W.; Chan S.H.; Lee S.-L.; NI-CHUNG LEE; Pfundt R.; Lau Y.-L.; Chung B.H. |
| 臺大學術典藏 |
2020-12-09T01:38:08Z |
Primary coenzyme Q10 deficiency-7: expanded phenotypic spectrum and a founder mutation in southern Chinese
|
Tse D.M.L.; Willis B.; Kwong A.K.-Y.; Chou Y.-Y.; Lin S.-P.; Quinzii C.M.; Hwu W.-L.; Chien Y.-H.; Kuo P.-L.; Chan V.C.-M.; Tsoi C.; Chong S.-C.; Rodenburg R.J.T.; Smeitink J.; Mak C.C.-Y.; Yeung K.-S.; Fung J.L.-F.; Lam W.; Hui J.; NI-CHUNG LEE; Fung C.-W.; Chung B.H.-Y.; Yu M.H.-C.; Tsang M.H.-Y.; Lai S.; Ho M.S.-P. |
| 國立成功大學 |
2019 |
Primary coenzyme Q10 deficiency-7: expanded phenotypic spectrum and a founder mutation in southern Chinese
|
Yu, M.H.-C.;Tsang, M.H.-Y.;Lai, S.;Ho, M.S.-P.;Tse, D.M.L.;Willis, B.;Kwong, A.K.-Y.;Chou, Y.-Y.;Lin, S.-P.;Quinzii, C.M.;Hwu, W.-L.;Chien, Y.-H.;Kuo, P.-L.;Chan, V.C.-M.;Tsoi, C.;Chong, S.-C.;Rodenburg, Rodenburg R.J.T.;Smeitink, J.;Mak, C.C.-Y.;Yeung, K.-S.;Fung, J.L.-F.;Lam, W.;Hui, J.;Lee, N.-C.;Fung, C.-W.;Chung, B.H.-Y. |
