Issue Date | Title | Author(s) | Source | scopus | WOS | Fulltext/Archive link |
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1993 | Cardiovascular disorders in Turner's syndrome and its correlation to karyotype. | Hou J.W.; WUH-LIANG HWU ; WEN-YU TSAI ; Lee J.S.; Wang T.R.; HUNG-CHI LUE | Journal of the Formosan Medical Association = Taiwan yi zhi | 22 | 0 | |
1991 | A clinical observation of achondroplasia. | WUH-LIANG HWU ; Wang T.R. | Zhonghua Minguo xiao er ke yi xue hui za zhi [Journal]. Zhonghua Minguo xiao er ke yi xue hui | 2 | 0 | |
1980 | Common variable immunodeficiency: An immunological study | KEH-SUNG TSAI ; Chuang C.Y.; Hsieh K.H.; Wang T.R.; KWEN-TAY LUH ; Hsu H.C. | Chinese Journal of Microbiology and Immunology | 0 | 0 | |
1991 | Crisis in Gaucher disease simulating osteomyelitis: report of one case. | Lai Y.C.; WUH-LIANG HWU ; Wang T.R.; Hsieh K.H.; CHIN-YUN LEE ; Li Y.W. | Acta Paediatrica Sinica | |||
1994 | Diagnosis of I-cell disease. | WUH-LIANG HWU ; Chuang S.C.; Wang W.C.; Wang T.R. | Zhonghua Minguo xiao er ke yi xue hui za zhi [Journal]. Zhonghua Minguo xiao er ke yi xue hui | 2 | 0 | |
1992 | DNA fingerprinting in the Chinese with an oligonucleotide probe (GTG)5. | WUH-LIANG HWU ; Chen R.L.; KAI-HSIN LIN ; Wang T.R. | Journal of the Formosan Medical Association = Taiwan yi zhi | 0 | 0 | |
1993 | 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. | Zhonghua Minguo xiao er ke yi xue hui za zhi [Journal]. Zhonghua Minguo xiao er ke yi xue hui | 3 | 0 | |
1994 | Fucosidosis in a Chinese girl | WUH-LIANG HWU ; Chuang S.C.; Wang W.C.; Wang T.R. | Journal of Inherited Metabolic Disease | 2 | 2 | |
1996 | Hepatoblastoma in an infant with Beckwith-Wiedemann Syndrome. | Tsai S.Y.; YUNG-MING JENG ; WUH-LIANG HWU ; YEN-HSUAN NI ; MEI-HWEI CHANG ; Wang T.R. | Journal of the Formosan Medical Association = Taiwan yi zhi | 8 | 3 | |
2000 | Identification and characterization of -3c-g acceptor splice site mutation in human α-L-iduronidase associated with mucopolysaccharidosis type IH/S | Teng Y.N.; Wang T.R.; WUH-LIANG HWU ; Lin S.P.; Lee-Chen G.J. | Clinical Genetics | 20 | 18 | |
1993 | In Vitro DNA Methylation Inhibits FMR-1 Promoter | WUH-LIANG HWU ; Lee Y.M.; Lee S.C.; Wang T.R. | Biochemical and Biophysical Research Communications | 34 | 36 | |
1993 | Maternal and fetal outcome of pregnant women with idiopathic thrombocytopenic purpura: retrospective analysis of 25 pregnancies. | HSIAO-LIN HWA ; RUEY-JIEN CHEN ; Chen Y.C.; Wang T.R.; Huang S.C.; SONG-NAN CHOW | Journal of the Formosan Medical Association = Taiwan yi zhi | 14 | ||
1992 | Measurement of urinary orotic acid by gas chromatography-mass spectrometry. | WUH-LIANG HWU ; Chou S.P.; Wang T.R. | Zhonghua Minguo xiao er ke yi xue hui za zhi [Journal]. Zhonghua Minguo xiao er ke yi xue hui | 3 | 0 | |
1995 | Microdeletion of chromosomal region 22q11 in DiGeorge syndrome: report of a case. | Hou J.W.; JOU-KOU WANG ; Chou C.C.; Wang T.R. | Journal of the Formosan Medical Association = Taiwan yi zhi | 3 | 0 | |
1995 | Molecular diagnosis of Gaucher disease type II. | Tsai F.J.; Chen H.W.; Peng C.T.; Tsai C.H.; WUH-LIANG HWU ; Wang T.R.; Liu S.C. | Zhonghua Minguo xiao er ke yi xue hui za zhi [Journal]. Zhonghua Minguo xiao er ke yi xue hui | 2 | 0 | |
1987 | Neonatal hepatitis: A follow-up study | MEI-HWEI CHANG ; Hsu H.C.; CHIN-YUN LEE ; Wang T.R.; CHUAN-LIANG KAO | Journal of Pediatric Gastroenterology and Nutrition | 47 | 32 | |
1991 | Niemann-Pick disease type B with ocular involvement: report of a case. | Tsai F.J.; Peng C.T.; Tsai C.H.; WUH-LIANG HWU ; Wang T.R. | Zhonghua Minguo xiao er ke yi xue hui za zhi [Journal]. Zhonghua Minguo xiao er ke yi xue hui | 0 | 0 | |
1996 | Oculomotor apraxia in a case of Gaucher's disease with homozygous T1448C mutation. | Tsai L.P.; Sue W.C.; WUH-LIANG HWU ; KAI-HSIN LIN ; Wang T.R. | Zhonghua Minguo xiao er ke yi xue hui za zhi [Journal]. Zhonghua Minguo xiao er ke yi xue hui | 7 | 0 | |
1991 | Prader-Willi syndrome with chromosome 15 interstitial deletion: report of one case. | WUH-LIANG HWU ; WEN-YU TSAI ; Lee J.S.; Wang P.J.; Wang T.R. | Acta Paediatrica Sinica | 3 | 0 | |
1991 | Quantification of arylsulfatase B activity and diagnosis of Maroteaux-Lamy syndrome. | WUH-LIANG HWU ; Wang T.R. | Zhonghua Minguo xiao er ke yi xue hui za zhi [Journal]. Zhonghua Minguo xiao er ke yi xue hui | 2 | 0 |