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Showing items 166-190 of 218  (9 Page(s) Totally)
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Institution Date Title Author
臺大學術典藏 2018-09-10T04:46:09Z Recurrent Down's syndrome due to maternal ovarian trisomy 21 mosaicism Tseng, L.-H.;Chuang, S.-M.;Lee, T.-Y.;Ko, T.-M.; LI-HUI TSENG
臺大學術典藏 2018-09-10T04:46:09Z Prevalence and molecular studies of thalassemia in five aboriginal groups in Taiwan. LI-HUI TSENG; Ko, T.M.;Tseng, L.H.;Cheng, T.A.;Hwa, H.L.;Chang, Y.K.;Chuang, S.M.;Lee, T.Y.
臺大學術典藏 2018-09-10T04:46:09Z Prenatal diagnosis of X-linked hydrocephalus in a Chinese family with four successive affected pregnancies Ko, T.-M.;Hwa, H.-L.;Tseng, L.-H.;Hsieh, F.-J.;Huang, S.-F.;Lee, T.-Y.; LI-HUI TSENG
臺大學術典藏 2018-09-10T04:44:43Z Evaluation of second trimester maternal serum screening for Down's syndrome using the Spiegelhalter-Knill-Jones (S-KJ) approach Hwa, H.-L.;Yen, M.-F.;Hsieh, F.-J.;Ko, T.-M.;Chen, T.H.-H.; HSIU-HSI CHEN; HSIAO-LIN HWA
臺大學術典藏 2018-09-10T04:42:48Z Prenatal diagnosis of mos46,X,del(Y)(q11.2)/45,X by cytogenetic and molecular studies with multiplex STR analysis Hwa, H.-L.;Ko, T.-M.;Chang, Y.-Y.;Huang, C.-H.;Su, Y.-N.;Tseng, L.-H.;Hsieh, F.-J.; LI-HUI TSENG; HSIAO-LIN HWA
臺大學術典藏 2018-09-10T04:07:04Z Dystrophin gene deletion in Chinese Duchenne/Becker muscular dystrophy patients via multiplex DNA amplification. Ko, T.M.;Tseng, L.H.;Chiu, H.C.;Hsieh, F.J.;Lee, T.Y.; LI-HUI TSENG
臺大學術典藏 2018-09-10T04:07:04Z Carrier detection and prenatal diagnosis of alpha-thalassemia of Southeast Asian deletion by polymerase chain reaction Ko, T.-M.;Tseng, L.-H.;Hsieh, F.-J.;Hsu, P.-M.;Lee, T.-Y.; LI-HUI TSENG
臺大學術典藏 2018-09-10T04:07:04Z Prenatal cytogenetic diagnosis in amniocentesis. Hsieh, F.J.;Ko, T.M.;Tseng, L.H.;Chang, L.S.;Pan, M.F.;Chuang, S.M.;Lee, T.Y.;Chen, H.Y.; LI-HUI TSENG
臺大學術典藏 2018-09-10T04:07:03Z Rapid prenatal determination of fetal sex by polymerase chain reaction on amniocyte DNA. Tseng, L.H.;Ko, T.M.;Hsieh, F.J.;Chuang, S.M.;Lee, T.Y.; LI-HUI TSENG
臺大學術典藏 2018-09-10T03:53:01Z Limb-reduction defects and chorion villus sampling Mastroiacovo, P.;Pontes Cavalcanti, D.;Monni, G.;Maria Ibba, R.;Lai, R.;Olla, G.;Cao, A.;Hsieh, F.-J.;Chen, D.;Tseng, L.-H.;Lee, C.-N.;Ko, T.-M.;Chuang, S.-M.;Chen, H.-Y.;Shepard, Thomash.;Kapur, Rajp.;Fantel, Alang.; LI-HUI TSENG; CHIEN-NAN LEE
臺大學術典藏 2018-09-10T03:43:03Z Selective reduction of multiple pregnancies in the first trimester or early second trimester. Ko, T.M.;Yang, Y.S.;Hsieh, F.J.;Ho, H.N.;Liu, C.H.;Tseng, L.H.;Chen, H.Y.;Lee, T.Y.; LI-HUI TSENG
臺大學術典藏 2012 Fifteen non-CODIS autosomal short tandem repeat loci multiplex data from nine population groups living in Taiwan Ko T.-M.; Su Y.-N.; Yin H.-Y.; Tseng L.-H.; Lin C.-Y.; Lee J.C.-I.; Chang Y.-Y.; HSIAO-LIN HWA
臺大學術典藏 2010 Seventeen Y-chromosomal short tandem repeat haplotypes in seven groups of population living in Taiwan Hsiao-Lin Hwa;Tseng L.-H.;Ko T.-M.;Chang Y.-Y.;Yin H.-Y.;Su Y.-N.;Lee J.C.-I.; HSIAO-LIN HWA; Tseng L.-H.; Ko T.-M.; Chang Y.-Y.; Yin H.-Y.; Su Y.-N.; Lee J.C.-I.
臺大學術典藏 2010 Seventeen Y-chromosomal short tandem repeat haplotypes in seven groups of population living in Taiwan JAMES CHUN-I LEE; Su Y.-N.; Yin H.-Y.; Chang Y.-Y.; Ko T.-M.; Tseng L.-H.; Hwa H.-L.; Hwa H.-L.;Tseng L.-H.;Ko T.-M.;Chang Y.-Y.;Yin H.-Y.;Su Y.-N.;James Chun-I Lee
臺大學術典藏 2009 Pseudogene-derived IKBKG gene mutations in incontinentia pigmenti Lee N.C.; Huang C.H.; Hwu W.L.; YIN-HSIU CHIEN; Chang Y.Y.; Chen C.H.; Ko T.M.
國立成功大學 2003-06-01 Modeling the stability of electroless plating bath - diffusion of nickel colloidal particles from the plating frontier Yin, X.; Hong, L.; Chen, B. H.; Ko, T. M.
國立成功大學 2003 A study on the interfacial composition of the electroless-copper-plated BPDA-PDA polyimide sheet Yu, W. X.; Hong, L.; Chen, Bing-Hung; Ko, T. M.
臺大學術典藏 2003 Genetic screening of karyotypes and azoospermic factors for infertile men who are candidates for ICSI Chang H.-C.; Yang Y.-S; HONG-NERNG HO; Ko T.-M; Chen S.-U; Lien Y.-R; Chen S.-U;Lien Y.-R;Ko T.-M;Hong-Nerng Ho;Yang Y.-S;Chang H.-C.
臺大學術典藏 1999 Ectopic pregnancy after tubal ligation [3] Ko T.-M.;Chang K.-J.;Lin F.-Y.;SHYR-CHYR CHEN;Huang J.-H.; Huang J.-H.; SHYR-CHYR CHEN; Lin F.-Y.; Chang K.-J.; Ko T.-M.
臺大學術典藏 1999 Molecular genetic study of Pompe disease in Chinese patients in Taiwan Ko T.-M.;Wuh-Liang Hwu;Lin Y.-W.;Tseng L.-H.;Hwa H.-L.;Wang T.-R.;Chuang S.-M.; Ko T.-M.; WUH-LIANG HWU; Lin Y.-W.; Tseng L.-H.; Hwa H.-L.; Wang T.-R.; Chuang S.-M.
臺大學術典藏 1998 Fluorescence microsatellite analysis to study the parental origin of the supernumerary chromosome in Down's syndrome Ko T.M.; HSIAO-LIN HWA; Tseng L.H.; Lin Y.W.; Cheung Y.P.
臺大學術典藏 1997 Misdiagnosis of homozygous alpha-thalassaemia 1 may occur if polymerase chain reaction alone is used in prenatal diagnosis Ko T.-M.;Tseng L.-H.;Hsiao-Lin Hwa;Hsu P.-M.;Li S.-F.;Chu J.-Y.;Lu P.-J.;Lee T.-Y.;Chuang S.-M.; Ko T.-M.; Tseng L.-H.; HSIAO-LIN HWA; Hsu P.-M.; Li S.-F.; Chu J.-Y.; Lu P.-J.; Lee T.-Y.; Chuang S.-M.
國立臺灣大學 1994 Amniocentesis in Mothers Who are Hepatitis B Virus Carriers Does not Expose the Infant to an Increased Risk of Hepatitis B Virus Infection Ko, T. M.; Tseng, L. H.; Chang, M. H.; 陳定信; Hsieh, F. J.; Chuang, S. M.; Lee, T. Y.; Ko, T. M.; Tseng, L. H.; Chang, M. H.; Chen, Ding-Shinn; Hsieh, F. J.; Chuang, S. M.; Lee, T. Y.
國立臺灣大學 1994 Infrequent Mutation in Tumor Suppressor Gene P53 in Gestational Trophoblastic Neoplasia Chen, C. A.; Chen, Y. H.; 陳擇銘; Ko, T. M.; Wu, C. C.; Lee, C. N.; 謝長堯; Chen, C. A.; Chen, Y. H.; Chen, Tzer-Ming; Ko, T. M.; Wu, C. C.; Lee, C. N.; Hsieh, Chang-Yao
臺大學術典藏 1994 Infrequent mutation in tumor suppressor gene p53 in gestational trophoblastic neoplasia Chen C.-A.; YEN-HUI CHEN; Chen T.-M.; Ko T.-M.; Wu C.-C.; Lee C.-N.; Hsieh C.-Y.

Showing items 166-190 of 218  (9 Page(s) Totally)
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