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Showing items 441-465 of 594 (24 Page(s) Totally)
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| 中國醫藥大學 |
2002 |
Hydrops foetalis caused by anti-Mur in first pregnancy - a case report
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Wu, KH; Chang, JG; Lin, M; Shih, MC; Lin, HC; Lee, CC; Peng, CT; Tsai, CH |
| 中國醫藥大學 |
2002 |
Hydrops foetalis caused by anti-Mur in first pregnancy - a case report
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Wu, KH; Chang, JG; Lin, M; Shih, MC; Lin, HC; Lee, CC; Peng, CT; Tsai, CH |
| 中國醫藥大學 |
2002 |
Environmental risk factors of young onset Parkinson's disease: a case-control study
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Tsai, CH; Lo, SK; See, LC; Chen, HZ; Chen, RS; Weng, YH; Chang, FC; Lu, CS |
| 中國醫藥大學 |
2002 |
Molecular analysis of syndromic congenital heart disease using short tandem repeat markers and semiquantitative polymerase chain reaction method
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Shi, YR; Hsieh, KS; Wu, JY; Lee, CC; Tsai, CH; Tsai, FJ |
| 中國醫藥大學 |
2002 |
Prognostic significance of the proline form of p53 codon 72 polymorphism in nasopharyngeal carcinoma
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Tsai, MH; Lin, CD; Hsieh, YY; Chang, FCC; Tsai, FJ; Chen, WC; Tsai, CH |
| 中山醫學大學 |
2001 |
The correlation between alteration of p16 gene and clinical status in oral squamous cell carcinoma.
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Tsai, CH; Yang, CC; Chou, LS; Chou, MY |
| 中山醫學大學 |
2001 |
The correlation between alteration of p16 gene and clinical status in oral squamous cell carcinoma.
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Tsai, CH; Yang, CC; Chou, LS; Chou, MY |
| 中國醫藥大學 |
2001 |
Androgen receptor trinucleotide polymorphism in endometriosis
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Hsieh, YY; Chang, CC; Tsai, FJ; Wu, JY; Tsai, CH; Tsai, HD |
| 中國醫藥大學 |
2001 |
Further evidence that fibroblast growth factor receptor 2 mutations cause Antley-Bixler syndrome
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Tsai, FJ; Wu, JY; Yang, CF; Tsai, CH |
| 中國醫藥大學 |
2001 |
Relation of polymorphism in the promotor region for the human osteocalcin gene to bone mineral density and occurrence of osteoporosis in postmenopausal Chinese women in Taiwan
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Chen, HY; Tsai, HD; Chen, WC; Wu, JY; Tsai, FJ; Tsai, CH |
| 中國醫藥大學 |
2001 |
Polymorphisms for interleukin-1 beta (IL-1 beta)-511 promoter, IL-1 beta exon 5, and IL-1 receptor antagonist: Nonassociation with endometriosis
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Hsieh, YY; Chang, CC; Tsai, FJ; Wu, JY; Shi, YR; Tsai, HD; Tsai, CH |
| 中國醫藥大學 |
2001 |
p21 gene codon 31 arginine/serine polymorphism: Non-association with endometriosis
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Hsieh, YY; Tsai, FJ; Chang, CC; Chen, WC; Tsai, CH; Tsai, HD; Lin, CC |
| 中國醫藥大學 |
2001 |
Mutation analysis of Crouzon syndrome and identification of one novel mutation in Taiwanese patients
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Tsai, FJ; Yang, CF; Wu, JY; Tsai, CH; Lee, CC |
| 中國醫藥大學 |
2001 |
Rapid monitoring assay of congenital adrenal hyperplasia with microbore high-performance liquid chromatography/electrospray ionization tandem mass spectrometry from dried blood spots
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Lai, CC; Tsai, CH; Tsai, FJ; Lee, CC; Lin, WD |
| 中國醫藥大學 |
2001 |
Rapid monitoring assay of congenital adrenal hyperplasia with microbore high-performance liquid chromatography/electrospray ionization tandem mass spectrometry from dried blood spots
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Lai, CC; Tsai, CH; Tsai, FJ; Lee, CC; Lin, WD |
| 中國醫藥大學 |
2001 |
Leukemia inhibitory factor decreases the arylamine N-acetyltransferase activity in human cumulus granulosa cells
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Chang, CC; Hsieh, YY; Chung, JG; Tsai, HD; Tsai, CH |
| 中國醫藥大學 |
2001 |
Kinetics of acetyl coenzyme A: Arylamine N-acetyltransferase from human cumulus cells
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Chang, CC; Hsieh, YY; Chung, JG; Tsai, HD; Tsai, CH |
| 中國醫藥大學 |
2001 |
Kinetics of acetyl coenzyme A: Arylamine N-acetyltransferase from human cumulus cells
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Chang, CC; Hsieh, YY; Chung, JG; Tsai, HD; Tsai, CH |
| 中國醫藥大學 |
2001 |
Prenatal diagnosis of oculocutaneous albinism two mutations located at the same allele
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Hsieh, YY; Wu, JY; Chang, CC; Tsai, FJ; Lee, CC; Tsai, HD; Tsai, CH |
| 中國醫藥大學 |
2001 |
Prenatal diagnosis of oculocutaneous albinism two mutations located at the same allele
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Hsieh, YY; Wu, JY; Chang, CC; Tsai, FJ; Lee, CC; Tsai, HD; Tsai, CH |
| 中國醫藥大學 |
2001 |
Longitudinal survey of blood flow at three different locations in the middle cerebral artery in normal fetuses
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Hsieh, YY; Chang, CC; Tsai, HD; Tsai, CH |
| 中國醫藥大學 |
2001 |
Relation of BsmI vitamin D receptor gene polymorphism to bone mineral density and occurrence of osteoporosis in postmenopausal Chinese women in Taiwan
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Chen, HY; Chen, WC; Hsu, CD; Tsai, FJ; Tsai, CH; Li, CW |
| 中國醫藥大學 |
2001 |
Mutation analysis of a family with hereditary hemorrhagic telangiectasia associated with hepatic arteriovenous malformation
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Lin, WD; Wu, JY; Hsu, HB; Tsai, FJ; Lee, CC; Tsai, CH |
| 中國醫藥大學 |
2001 |
Mutation analysis of a family with hereditary hemorrhagic telangiectasia associated with hepatic arteriovenous malformation
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Lin, WD; Wu, JY; Hsu, HB; Tsai, FJ; Lee, CC; Tsai, CH |
| 中國醫藥大學 |
2001 |
Molecular analysis of SMN, NAIP and P44 genes of SMA patients and their families
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Tsai, CH; Jong, YJ; Hu, CJ; Chen, CM; Shih, MC; Chang, CP; Chang, JG |
Showing items 441-465 of 594 (24 Page(s) Totally)
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