|
English
|
正體中文
|
简体中文
|
2828323
|
|
???header.visitor??? :
32195113
???header.onlineuser??? :
6290
???header.sponsordeclaration???
|
|
|
|
???tair.name??? >
???browser.page.title.author???
|
"tsai lp"???jsp.browse.items-by-author.description???
Showing items 1-7 of 7 (1 Page(s) Totally)
1
View [10|25|50] records per page
| 中山醫學大學 |
2021 |
Epigenotype, Genotype, and Phenotype Analysis of Taiwanese Patients with Silver-Russell Syndrome
|
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
|
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.
|
(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.
|
(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
|
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.
|
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
|
Wu, JY; Lin, SP; Tsai, LP; Tsai, FJ; Peng, CT; Tsai, CH |
Showing items 1-7 of 7 (1 Page(s) Totally)
1
View [10|25|50] records per page
|
