| 國立成功大學 |
2023 |
Critical body fat percentage required for puberty onset: the Taiwan Pubertal Longitudinal Study
|
Huang, L.;Hou, J.-W.;Fan, H.-Y.;Tsai, M.-C.;Yang, C.;Hsu, J.B.;Chen, Y.C. |
| 臺大學術典藏 |
2022-07-15T10:33:46Z |
Corneal opacity and congenital glaucoma associated with massive heparan sulfaturia: report of one case
|
Lin, S C; FUNG-RONG HU; Hou, J W; Yao, Y T; Wang, T R; Hung, P T |
| 臺大學術典藏 |
2022-06-27T06:59:31Z |
Prediction of Mandibular Advancement Device Response Using CPAP Pressure in Different Polysomnographic Phenotypes
|
Lee C.-F.; Chen Y.-J.; Huang W.-C.; Hou J.-W.; Liu Y.-T.; Shih T.T.-F.; Lee P.-L.; CHONG-JEN YU |
| 臺大學術典藏 |
2022-04-08T09:23:14Z |
Recurrent chemical reactivations of EBV promotes genome instability and enhances tumor progression of nasopharyngeal carcinoma cells
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Fang C.-Y.; Lee C.-H.; Wu C.-C.; Chang Y.-T.; Yu S.-L.; Chou S.-P.; Huang P.-T.; Chen C.-L.; Hou J.-W.; Chang Y.; CHING-HWA TSAI; Takada K.; Chen J.-Y. |
| 國立成功大學 |
2022 |
Critical body fat percentage required for puberty onset: the Taiwan Pubertal Longitudinal Study
|
Huang, L.;Hou, J.-W.;Fan, H.-Y.;Tsai, M.-C.;Yang, C.;Hsu, J.B.;Chen, Y.C. |
| 臺大學術典藏 |
2021-07-02T03:41:35Z |
The difference in immune response and IL-12p35 methylation between newborns and adults
|
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
|
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.
|
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
|
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]
|
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.
|
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
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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)
|
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.
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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
|
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. |
