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Showing items 1-7 of 7 (1 Page(s) Totally)
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| 中山醫學大學 |
2021 |
Epigenotype, Genotype, and Phenotype Analysis of Taiwanese Patients with Silver-Russell Syndrome
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Lin, HY; Lee, CL; Fran, S; Tu, RY; Chang, YH; Niu, DM; Chang, CY; Chiu, PC; Chou, YY; Hsiao, HP; Tsai, MC; Chao, MC; Tsai, LP; Yang, CF; Su, PH; Pan, YW; Lee, CH; Chu, TH; Chuang, CK; Lin, SP |
| 國家衛生研究院 |
2009-05 |
A novel microdeletion at chromosome 2q31.1-31.2 in a three-generation family presenting duplication of great toes with clinodactyly
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Tsai, LP;Liao, HM;Chen, YJ;Fang, JS;Chen, CH |
| 中國醫藥大學 |
2003.06 |
Mutation of IVS2-12A/C > G in combination with 707-714delGAGACTAC in the CYP21 gene is caused by deletion of the C4-CYP21 repeat module with steroid 21-hydroxylase deficiency.
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(Lee HH); (Chang SF); 蔡輔仁(Fuu-Jen Tsai); (Tsai LP); (Lin CY) |
| 中國醫藥大學 |
2003.06 |
Mutation of IVS2-12A/C > G in combination with 707-714delGAGACTAC in the CYP21 gene is caused by deletion of the C4-CYP21 repeat module with steroid 21-hydroxylase deficiency.
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(Lee HH); (Chang SF); 蔡輔仁(Fuu-Jen Tsai); (Tsai LP); (Lin CY) |
| 中國醫藥大學 |
2003 |
Mutation of IVS2-12A/C > G in combination with 707-714delGAGACTAC in the CYP21 gene is caused by deletion of the C4-CYP21 repeat module with steroid 21-hydroxylase deficiency
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Lee, HH; Chang, SF; Tsai, FJ; Tsai, LP; Lin, CY |
| 中國醫藥大學 |
2001 |
Haplotype analysis in patients with velopharyngeal insufficiency (VPI) minimizes one VPI locus in 2.8Mb region of 22q11.
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Tsai, LP; Tsou, KS; Shi, YR; Wu, JY; Tsai, FJ |
| 中國醫藥大學 |
1998 |
Molecular analysis of type I oculocutaneous albinism in Chinese
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Wu, JY; Lin, SP; Tsai, LP; Tsai, FJ; Peng, CT; Tsai, CH |
Showing items 1-7 of 7 (1 Page(s) Totally)
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