臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)

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	2019臺灣學術機構典藏研討會
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Institution	Date	Title	Author
臺大學術典藏	2018-09-10T08:06:33Z	Seventeen Y-chromosomal short tandem repeat haplotypes in seven groups of population living in Taiwan	Hwa, H.-L.;Tseng, L.-H.;Ko, T.-M.;Chang, Y.-Y.;Yin, H.-Y.;Su, Y.-N.;Lee, J.C.-I.; LI-HUI TSENG; JAMES CHUN-I LEE; HSIAO-LIN HWA
臺大學術典藏	2018-09-10T07:24:56Z	Molecular genetic study of Pompe disease in Chinese patients in Taiwan	Ko, T.-M.;Hwu, W.-L.;Lin, Y.-W.;Tseng, L.-H.;Hwa, H.-L.;Wang, T.-R.;Chuang, S.-M.; LI-HUI TSENG; HSIAO-LIN HWA
臺大學術典藏	2018-09-10T07:24:56Z	Erratum: Molecular genetic study of Pompe disease in Chinese patients in Taiwan (Human Mutation (1999) 13 (380-384))	Ko, T.-M.;Hwu, W.-L.;Lin, Y.-W.;Tseng, L.-H.;Hwa, H.-L.;Wang, T.-R.;Chuang S.-, M.;Hayashi, K.; LI-HUI TSENG; HSIAO-LIN HWA
臺大學術典藏	2018-09-10T07:24:56Z	Erratum: Molecular characterization and PCR diagnosis of Thailand deletion of α-globin gene cluster (American Journal of Hematology (1998) (124-130))	Ko, T.-M.;Tseng, L.-H.;Kao, C.-H.;Lin, Y.-W.;Hwa, H.-L.;Hsu, P.-M.;Li S.-, F.;Chuang, S.-M.; LI-HUI TSENG; HSIAO-LIN HWA
臺大學術典藏	2018-09-10T06:17:20Z	Misdiagnosis of homozygous alpha-thalassaemia 1 may occur if polymerase chain reaction alone is used in prenatal diagnosis	Ko, T.-M.;Tseng, L.-H.;Hwa, H.-L.;Hsu, P.-M.;Li, S.-F.;Chu, J.-Y.;Lu, P.-J.;Lee, T.-Y.;Chuang, S.-M.; LI-HUI TSENG; HSIAO-LIN HWA
臺大學術典藏	2018-09-10T06:06:47Z	A novel heterozygous missense mutation 377T > C (V126A) of TGIF gene in a family segregated with holoprosencephaly and moyamoya disease	Chen, M.;Kuo, S.-J.;Liu, C.-S.;Chen, W.-L.;Ko, T.-M.;Chen, T.-H.;Chang, S.-P.;Huang, C.-H.;Chang, Y.-Y.;Wang, B.-T.; MING CHEN
臺大學術典藏	2018-09-10T05:48:59Z	Norplant® subdermal contraceptive system: Experience in Taiwan	Tseng, L.-H.;Lee, T.-Y.;Yang, Y.-S.;Ko, T.-M.;Chuang, S.-M.; LI-HUI TSENG; YU-SHIH YANG
臺大學術典藏	2018-09-10T05:14:34Z	Ultrasonographic scanning of placental thickness and the prenatal diagnosis of homozygous alpha-thalassaemia 1 in the second trimester	LI-HUI TSENG; HSIAO-LIN HWA; Ko, T.-M.;Tseng, L.-H.;Hsu, P.-M.;Hwa, H.-L.;Lee, T.-Y.;Chuang, S.-M.
臺大學術典藏	2018-09-10T05:14:34Z	Prenatal diagnosis by transabdominal chorionic villus sampling in the second and third trimesters	Ko, T.-M.;Tseng, L.-H.;Hwa, H.-L.;Lee, T.-Y.;Chuang, S.-M.; LI-HUI TSENG; HSIAO-LIN HWA
臺大學術典藏	2018-09-10T04:46:10Z	Cytogenetic study of spontaneous abortions with the Giemsa banding method.	Hwa, H.L.;Tseng, L.H.;Ho, H.N.;Ko, T.M.; LI-HUI TSENG
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.

Showing items 156-180 of 218 (9 Page(s) Totally)
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