臺大學術典藏 |
2021-07-02T03:41:35Z |
The difference in immune response and IL-12p35 methylation between newborns and adults
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Chen C.-J.; Hou J.-W.; BOR-LUEN CHIANG |
臺大學術典藏 |
2021-06-29T08:16:07Z |
Kleine-Levin syndrome in a boy with Prader-Willi syndrome
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Gau S.-F.; Soong W.-T.; Liu H.-M.; Hou J.-W.; Tsai W.-Y.; YEN-NAN CHIU; Yeh Y.-C.; Wang P.-J.; Wang T.-R. |
臺大學術典藏 |
2021-06-11T02:56:22Z |
Trisomy 18 in a patient with CHARGE association.
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WANG-TSO LEE; Hou J.W.; Yau K.I.; Wang T.R. |
臺大學術典藏 |
2021-01-08T02:16:47Z |
Homocystinuria presenting as fatal common carotid artery occlusion
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Chiu H.-H.; Wang T.-R.; Wang P.-J.; Hou J.-W.; CHUN-YI LU; Chun-Yi Lu;Hou J.-W.;Wang P.-J.;Chiu H.-H.;Wang T.-R. |
臺大學術典藏 |
2021-01-08T02:16:46Z |
Bifid tongue associated with midline cleft palate, mandible, cervical vertebrae and linea alba [2]
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Cheng T.-J.; Hou J.-W.; CHUN-YI LU; Teng R.-J. |
臺大學術典藏 |
2021-01-06T05:51:04Z |
Microdeletion of chromosomal region 22q11 in DiGeorge syndrome: report of a case.
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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
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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
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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)
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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)
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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
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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.
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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
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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
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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
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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.
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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.
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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.
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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
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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)
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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
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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
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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
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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
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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
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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. |