| 臺大學術典藏 |
2021-01-06T05:51:04Z |
Microdeletion of chromosomal region 22q11 in DiGeorge syndrome: report of a case.
|
Hou J.W.; Hou J.W.;Jou-Kou Wang;Chou C.C.;Wang T.R.; JOU-KOU WANG; Chou C.C.; Wang T.R. |
| 臺大學術典藏 |
2021-01-06T05:51:00Z |
Microdeletion of chromosomal region 7q11.23 in Willias syndrome
|
Hou J.-W.;Jou-Kou Wang;Wang T.-R.; Hou J.-W.; JOU-KOU WANG; Wang T.-R. |
| 臺大學術典藏 |
2021-01-06T05:51:00Z |
CATCH 22: Deletion of locus 22Q11 in velocardiofacial syndrome, digeorge anomaly, and nonsyndromic conotruncal defects
|
Hou J.-W.; JOU-KOU WANG; Tsai W.-Y.; Chou C.-C.; Wang T.-R. |
| 臺大學術典藏 |
2021-01-06T05:50:54Z |
Congenital contractural arachnodactyly (Beals syndrome)
|
Su P.-H.;Hou J.-W.;Hwu W.-L.;Wu M.-H.;Jou-Kou Wang;Wang T.-R.; Su P.-H.; Hou J.-W.; Hwu W.-L.; Wu M.-H.; JOU-KOU WANG; Wang T.-R. |
| 臺大學術典藏 |
2021-01-05T08:07:57Z |
Congenital contractural arachnodactyly (Beals syndrome)
|
Su P.-H.;Hou J.-W.;Hwu W.-L.;Mei-Hwan Wu;Wang J.-K.;Wang T.-R.; Su P.-H.; Hou J.-W.; Hwu W.-L.; MEI-HWAN WU; Wang J.-K.; Wang T.-R. |
| 臺大學術典藏 |
2021-01-04T12:13:07Z |
Jacobsen distal 11q deletion syndrome with a myelodysplastic change of hemopoietic cells
|
Hou J.-W.; Teng R.-J.; HWEI-FANG TIEN; Lin K.-H. |
| 臺大學術典藏 |
2021-01-04T07:41:16Z |
Kawasaki disease complicated by gallbladder hydrops mimicking acute abdomen: a report of three cases.
|
Lee C.Y.; Wu M.H.; Hou J.W.; MEI-HWEI CHANG |
| 臺大學術典藏 |
2021-01-04T07:38:41Z |
Metabolic disorders mimicking Reye's syndrome
|
Chang P.-F.;Huang S.-F.;Hwu W.-L.;Hou J.-W.;Ni Y.-H.;Mei-Hwei Chang; Chang P.-F.; Huang S.-F.; Hwu W.-L.; Hou J.-W.; Ni Y.-H.; MEI-HWEI CHANG |
| 臺大學術典藏 |
2020-12-28T08:15:08Z |
Metabolic disorders mimicking Reye's syndrome
|
Chang P.-F.; Chang P.-F.;Huang S.-F.;Hwu W.-L.;Hou J.-W.;Yen-Hsuan Ni;Chang M.-H.; Huang S.-F.; Hwu W.-L.; Hou J.-W.; YEN-HSUAN NI; Chang M.-H. |
| 臺大學術典藏 |
2020-12-18T02:21:57Z |
Electroclinical characteristics of seizures - Comparing Prader-Willi syndrome with Angelman syndrome
|
Wang P.-J.;Hou J.-W.;Sue W.-C.;Wang-Tso Lee; Wang P.-J.; Hou J.-W.; Sue W.-C.; WANG-TSO LEE |
| 臺大學術典藏 |
2020-12-16T02:26:31Z |
Y-specific polymerase chain reaction for the interpretation of a chromosome marker.
|
Wang T.R.;Wuh-Liang Hwu;Hou J.W.;Tsai H.M.;Liu C.H.; Wang T.R.; WUH-LIANG HWU; Hou J.W.; Tsai H.M.; Liu C.H. |
| 臺大學術典藏 |
2020-12-16T02:26:31Z |
Cardiovascular disorders in Turner's syndrome and its correlation to karyotype.
|
Hou J.W.; WUH-LIANG HWU; Tsai W.Y.; Lee J.S.; Wang T.R.; Lue H.C. |
| 臺大學術典藏 |
2020-12-16T02:26:30Z |
Fragile-X mental retardation--a combination of cytogenetic and molecular approaches, with greater emphasis on DNA analysis.
|
Wang T.R.;Wuh-Liang Hwu;Hou J.W.;Chou S.P.;Liu C.H.; Wang T.R.; WUH-LIANG HWU; Hou J.W.; Chou S.P.; Liu C.H. |
| 臺大學術典藏 |
2020-12-16T02:26:22Z |
Metabolic disorders mimicking Reye's syndrome
|
Chang P.-F.;Huang S.-F.;Wuh-Liang Hwu;Hou J.-W.;Ni Y.-H.;Chang M.-H.; Chang P.-F.; Huang S.-F.; WUH-LIANG HWU; Hou J.-W.; Ni Y.-H.; Chang M.-H. |
| 臺大學術典藏 |
2020-12-16T02:26:22Z |
Congenital contractural arachnodactyly (Beals syndrome)
|
Su P.-H.;Hou J.-W.;Wuh-Liang Hwu;Wu M.-H.;Wang J.-K.;Wang T.-R.; Su P.-H.; Hou J.-W.; WUH-LIANG HWU; Wu M.-H.; Wang J.-K.; Wang T.-R. |
| 臺大學術典藏 |
2020-12-08T03:29:03Z |
Tricho-rhino-phalangeal syndrome type II associated with epiglottic aplasia and congenital nephrotic syndrome
|
Frank Leigh Lu;Hou J.-W.;Tsai W.-S.;Teng R.-J.;Yau K.-I.T.;Wang T.-R.; FRANK LEIGH LU; Hou J.-W.; Tsai W.-S.; Teng R.-J.; Yau K.-I.T.; Wang T.-R. |
| 臺大學術典藏 |
2020-08-21T08:51:30Z |
Kleine-Levin syndrome in a boy with Prader-Willi syndrome
|
Gau S.-F.;Soong W.-T.;Hon-Man Liu;Hou J.-W.;Tsai W.-Y.;Chiu Y.-N.;Yeh Y.-C.;Wang P.-J.;Wang T.-R.; Gau S.-F.; Soong W.-T.; HON-MAN LIU; Hou J.-W.; Tsai W.-Y.; Chiu Y.-N.; Yeh Y.-C.; Wang P.-J.; Wang T.-R. |
| 臺大學術典藏 |
2020-07-01T08:53:41Z |
Optimization of walking in children
|
Suh-Fang Jeng;Liao H.-F.;Lai J.-S.;Hou J.-W.; SUH-FANG JENG; Liao H.-F.; Lai J.-S.; Hou J.-W. |
| 臺大學術典藏 |
2020-06-16T06:38:50Z |
Automatic Sleep Staging in Patients With Obstructive Sleep Apnea Using Single-Channel Frontal EEG
|
Lee, P.-L.;Huang, Y.-H.;Lin, P.-C.;Chiao, Y.-A.;Hou, J.-W.;Liu, H.-W.;Huang, Y.-L.;Liu, Y.-T.;Chiueh, T.-D.; Lee, P.-L.; Huang, Y.-H.; Lin, P.-C.; Chiao, Y.-A.; Hou, J.-W.; Liu, H.-W.; Huang, Y.-L.; Liu, Y.-T.; Chiueh, T.-D.; TZI-DAR CHIUEH |
| 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 |
2020-02-03T08:15:19Z |
Gene dosage change of TPTE and BAGE2 and breakpoint analysis in Robertsonian Down syndrome
|
Shaw S.-W.; Chen C.-P.; Cheng P.-J.; Wang T.-H.; Hou J.-W.; Lin C.-T.; Chang S.-D.; HSIAO-LIN HWA; Lin J.-L.; Chao A.-S.; Soong Y.-K.; Hsieh F.-J. |
| 臺大學術典藏 |
2019 |
Automatic sleep staging in patients with obstructive sleep apnea using single-channel frontal EEG
|
Pei-Lin Lee;Huang Y.-H.;Lin P.-C.;Chiao Y.-A.;Hou J.-W.;Liu H.-W.;Huang Y.-L.;Liu Y.-T.;Chiueh T.-D.; PEI-LIN LEE; Huang Y.-H.; Lin P.-C.; Chiao Y.-A.; Hou J.-W.; Liu H.-W.; Huang Y.-L.; Liu Y.-T.; Chiueh T.-D. |
| 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 |
2018-09-10T07:22:20Z |
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 |
2018-09-10T07:13:11Z |
Jacobsen distal 11q deletion syndrome with a myelodysplastic change of hemopoietic cells
|
Hou, J.-W.;Teng, R.-J.;Tien, H.-F.;Lin, K.-H.; KAI-HSIN LIN |
