|
"simmer j p"的相關文件
顯示項目 21-30 / 30 (共3頁)
<< < 1 2 3
每頁顯示[10|25|50]項目
| 臺大學術典藏 |
2021-07-06T09:59:58Z |
Transcriptome analysis of gingival tissues of enamel-renal syndrome
|
Wang Y.-P.;Lin H.-Y.;Zhong W.-L.;Simmer J.P.;Shih-Kai Wang; Wang Y.-P.; Lin H.-Y.; Zhong W.-L.; Simmer J.P.; SHIH-KAI Wang |
| 臺大學術典藏 |
2021-07-06T09:59:58Z |
ENAM mutations and digenic inheritance
|
Zhang H.;Hu Y.;Seymen F.;Koruyucu M.;Kasimoglu Y.;Shih-Kai Wang;Wright J.T.;Havel M.W.;Zhang C.;Kim J.-W.;Simmer J.P.;Hu J.C.C.; Zhang H.; Hu Y.; Seymen F.; Koruyucu M.; Kasimoglu Y.; SHIH-KAI Wang; Wright J.T.; Havel M.W.; Zhang C.; Kim J.-W.; Simmer J.P.; Hu J.C.C. |
| 臺大學術典藏 |
2021-07-06T09:59:57Z |
FAM83H and Autosomal Dominant Hypocalcified Amelogenesis Imperfecta
|
SHIH-KAI Wang; Zhang H.; Hu C.Y.; Liu J.F.; Chadha S.; Kim J.W.; Simmer J.P.; Hu J.C.C. |
| 臺大學術典藏 |
2021-07-05T07:35:47Z |
Taurodontism, variations in tooth number, and misshapened crowns in wnt10a null mice and human kindreds
|
Yang J.; Wang S.-K.; Choi M.; Reid B.M.; Hu Y.; YUAN-LING LEE; Herzog C.R.; Kim-Berman H.; Lee M.; Benke P.J.; Kent Lloyd K.C.; Simmer J.P.; Hu J.C.-C. |
| 臺大學術典藏 |
2021-07-05T07:35:47Z |
Fam83h null mice support a neomorphic mechanism for human ADHCAI
|
Wang S.-K.;Hu Y.;Yang J.;Smith C.E.;Richardson A.S.;Yamakoshi Y.;Yuan-Ling Lee;Seymen F.;Koruyucu M.;Gencay K.;Lee M.;Choi M.;Kim J.-W.;Hu J.C.-C.;Simmer J.P.; Wang S.-K.; Hu Y.; Yang J.; Smith C.E.; Richardson A.S.; Yamakoshi Y.; YUAN-LING LEE; Seymen F.; Koruyucu M.; Gencay K.; Lee M.; Choi M.; Kim J.-W.; Hu J.C.-C.; Simmer J.P. |
| 臺大學術典藏 |
2018-09-10T15:00:53Z |
STIM1 and SLC24A4 Are Critical for Enamel Maturation
|
Wang, S.;Choi, M.;Richardson, A.S.;Reid, B.M.;Seymen, F.;Yildirim, M.;Tuna, E.;Gen?Ay, K.;Simmer, J.P.;Hu, J.C.; SHIH-KAI Wang |
| 臺大學術典藏 |
2018-09-10T15:00:52Z |
Ameloblast transcriptome changes from secretory to maturation stages
|
Simmer, J.P.;Richardson, A.S.;Wang, S.-K.;Reid, B.M.;Bai, Y.;Hu, Y.;Hu, J.C.-C.; SHIH-KAI Wang |
| 臺大學術典藏 |
2018-09-10T15:00:52Z |
FAM20A mutations associated with enamel renal syndrome
|
Wang, S.K.;Reid, B.M.;Dugan, S.L.;Roggenbuck, J.A.;Read, L.;Aref, P.;Taheri, A.P.H.;Yeganeh, M.Z.;Simmer, J.P.;Hu, J.C.-C.; SHIH-KAI Wang |
| 臺大學術典藏 |
2018-09-10T15:00:52Z |
ITGB6 loss-of-function mutations cause autosomal recessive amelogenesis imperfecta
|
Wang, S.;Choi, M.;Richardson, A.S.;Reid, B.M.;Lin, B.P.;Wang, S.J.;Kim, J.;Simmer, J.P.;Hu, J.C.-C.; SHIH-KAI Wang |
| 臺大學術典藏 |
2018-09-10T08:47:44Z |
Enamel malformations associated with a defined dentin sialophosphoprotein mutation in two families
|
SHIH-KAI Wang; Wang, S.-K.;Chan, H.-C.;Rajderkar, S.;Milkovich, R.N.;Uston, K.A.;Kim, J.-W.;Simmer, J.P.;Hu, J.C.-C. |
顯示項目 21-30 / 30 (共3頁)
<< < 1 2 3
每頁顯示[10|25|50]項目
|
