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Showing items 41-65 of 78  (4 Page(s) Totally)
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Institution Date Title Author
中國醫藥大學 2006 Spectral karyotyping and fluorescence in situ hybridization analysis of de novo partial trisomy 7p (7p21.2pter) and partial monosomy 12q (12q24.33qter) 陳持平(Chen CP,); (Lin SP,); 林齊強(Lin CC,); 李月君(Li YC,); 謝麗嬌(Hsieh LJ,); (Huang JK,); (Lee CC,); (Wang W..)
中國醫藥大學 2006 Molecular cytogenetic analysis of de novo dup(5)(q35.2q35.3) and review of the literature of pure partial trisomy-5q. 陳持平(Chen CP,); (Lin SP,); 林齊強(Lin CC,); (Chen YJ,); (Chern SR,); 李月君(Li YC,); 謝麗嬌(Hsieh LJ,); (Lee CC,); (Wang W.)
中國醫藥大學 2006 Molecular cytogenetic analysis of de novo dup(5)(q33.1q31.1) associated with abnormal perinatal findings. (Chen CP); (Lin SP,); (Chern SR); 林齊強(Chyi-Chyang Lin); (Li YC,); (Lee CC); 謝麗嬌(Lie-Jiau Hsieh); (Chen WL,); (Wang W)
中國醫藥大學 2005 Perinatal finding and molecular cytogenetic analysis of de novo partial trisomy 16q (16q22.1→qter) and partial monosomy 20q (20q13.3→qter). 陳持平(Chen CP,); (Lin SP,); 林齊強(Lin CC,); (Li YC,); (Chern SR,); (Chen WM,); (Lee CC,); 謝麗嬌(Hsieh LJ,)
中國醫藥大學 2005 Distal 3p monosomy associated with epilepsy in a boy Chen, CP; Lin, SP; Ho, CS; Chern, SR; Lee, CC; Chen, WL; Wang, W
中國醫藥大學 2005 Spectral karyotyping, fluorescence in situ hybridization and molecular genetic analysis of de novo partial trisomy 7p (7p15.1 -> pter) and partial monosomy 9p (9p22 -> pter) Chen, CP; Lin, SP; Lin, CC; Li, YC; Hsieh, LJ; Chern, SR; Lee, CC; Chen, YJ; Wang, WS
中國醫藥大學 2005 Prenatal magnetic resonance imaging demonstration of the systemic feeding artery of a pulmonary sequestration associated with in utero regression Chen, CP; Liu, YP; Lin, SP; Sheu, JC; Hsu, CY; Chang, TY; Wang, W
中國醫藥大學 2005 Prenatal magnetic resonance imaging of Galloway-Mowat syndrome Chen, CP; Chang, TY; Lin, SP; Huang, JK; Tsai, JD; Chiu, NC; Wang, WS
中國醫藥大學 2005 A paternally derived inverted duplication of distal 14q with a terminal 14q deletion Chen, CP; Chern, SR; Lin, SP; Lin, CC; Li, YC; Wang, TH; Lee, CC; Pan, CW; Hsieh, LJ; Wang, WS
中國醫藥大學 2005 Prenatal diagnosis, sonographic findings and molecular genetic analysis of a 46,XX/46,XY true hermaphrodite chimera Chen, CP; Chern, SR; Sheu, JC; Lin, SP; Hsu, CY; Chang, TY; Lee, CC; Wang, W; Chen, HEC
中國醫藥大學 2005 Perinatal findings and molecular cytogenetic analysis of de novo partial trisomy 16q (16q22.1 -> qter) and partial monosomy 20q (20q13.3 -> qter) Chen, CP; Lin, SP; Lin, CC; Li, YC; Chern, SR; Chen, WM; Lee, CC; Hsieh, LJ; Wang, WS
中國醫藥大學 2005 Perinatal findings and molecular cytogenetic analysis of de novo partial trisomy 16q (16q22.1 -> qter) and partial monosomy 20q (20q13.3 -> qter) Chen, CP; Lin, SP; Lin, CC; Li, YC; Chern, SR; Chen, WM; Lee, CC; Hsieh, LJ; Wang, WS
中國醫藥大學 2005 Bioavailability and metabolic pharmacokinetics of rutin and quercetin in rats Yang, CY; Hsiu, SL; Wen, KC; Lin, SP; Tsai, SY; Hou, YC; Chao, PDL
中國醫藥大學 2005 Spectral karyotyping and fluorescence in situ hybridization analysis of de novo partial duplication of Yq (Yq11.2 -> qter) and partial monosomy 5p (5pl5.3 -> pter) Chen, CP; Lin, SP; Lin, CC; Li, YC; Hsieh, LJ; Lee, CC; Chen, YJ; Wang, W
中國醫藥大學 2005 Perinatal findings of partial trisomy 13q (13q14.1 -> qter) resulting from paternal pericentric inversion of chromosome 13 Chen, CP; Lin, SP; Lee, CC; Chen, WL; Chen, LF; Wang, WS
國家衛生研究院 2004-07 Description of the transcriptomes of immune response-activated Hemocytes from the mosquito vectors Aedes aegypti and Armigeres subalbatus Bartholomay, LC; Cho, WL; Rocheleau, TA; Boyle, JP; Beck, ET; Fuchs, JF; Liss, P; Rusch, M; Butler, KM; Wu, RCC; Lin, SP; Kuo, FY; Tsao, IY; Huang, CY; Liu, TT; Hsiao, KJ; Tsai, SF; Yang, UC; Nappi, AJ; Perna, NT; Chen, CC; Christensen, BM
國立臺灣大學 2004-03 DiGeorge syndrome with truncus arteriosus: report of one case. Liang, PH; Chen, MR; Shyur, SD; Lee, YJ; Lin, SP; Yu, MT; Chiu, IS; Chen, SJ
臺北醫學大學 2004 A comparative study of various histone deacetylase inhibitors on the proliferation, differentiation and apoptosis of human acute myeloid leukemia 劉興璟; Lin SP; Huang MJ; Liu CR; Chow JM; Lin CP; Liu HE
中國醫藥大學 2004 Detection of a homozygous D645E mutation of the acid alpha-glucosidase gene and glycogen deposition in tissues in a second-trimester fetus with infantile glycogen storage disease type II Chen, CP; Lin, SP; Tzen, CY; Tsai, FJ; Hwu, WL; Wan, WS
中國醫藥大學 2003 Prenatal identification of a G338E mutation in FGFR2 in a fetus without sonographic appearance of craniosynostosis Chen, CP; Chern, SR; Lin, SP; Wang, WS; Tsai, FJ
高雄醫學大學 2002 單側性腎臟多發囊腫症--病例報告及文獻回顧  林士弼;張哲銘;陳鴻鈞;賴永勳 ; Lin SP;Chang JM;Chen HC;Lai YH. 
高雄醫學大學 2002 Acyclovir-induced 造成之急性腎衰竭  郭美娟;張哲銘;林士弼;李佳蓉;陳鴻鈞;賴永勳 ; Kuo MC;Chang JM;Lin SP;Lee JJ;Chen HC;Lai YH. 
國立暨南國際大學 2001 我國國民中小學學校行政規則現況之探討 林淑萍; Lin, SP
中國醫藥大學 2001 Mucopolysaccharidosis type VI: Report of two Taiwanese patients and identification of one novel mutation Yang, CF; Wu, JY; Lin, SP; Tsai, FJ
中國醫藥大學 2000 Mutation analysis of type 2 Gaucher disease in Taiwan Chinese and identification of two novel mutations. Tsai, FJ; Wu, JY; Lin, SP; Chang, JG; Lee, CC; Tsai, CH

Showing items 41-65 of 78  (4 Page(s) Totally)
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