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Showing items 151-175 of 253 (11 Page(s) Totally)
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Institution	Date	Title	Author
臺大學術典藏	2020-02-03T08:15:29Z	Prevalence and molecular studies of thalassemia in five aboriginal groups in Taiwan.	Ko T.M.;Tseng L.H.;Cheng T.A.;Hsiao-Lin Hwa;Chang Y.K.;Chuang S.M.;Lee T.Y.; Ko T.M.; Tseng L.H.; Cheng T.A.; HSIAO-LIN HWA; Chang Y.K.; Chuang S.M.; Lee T.Y.
臺大學術典藏	2020-02-03T08:15:28Z	Sonographic manifestation and Doppler blood flow study in fetal triploidy syndrome: Report of two cases	Pan M.-F.; Tseng L.-H.; Hsieh F.-J.; Wu R.-T.;Shyu M.-K.;Lee C.-N.;Wu C.-C.;Hsiao-Lin Hwa;Lin C.-J.;Chen - F.C.;Chang L.-S.;Pan M.-F.;Tseng L.-H.;Hsieh F.-J.; Wu R.-T.; Shyu M.-K.; Lee C.-N.; Wu C.-C.; HSIAO-LIN HWA; Lin C.-J.; Chen - F.C.; Chang L.-S.
臺大學術典藏	2020-02-03T08:15:28Z	Increased level of second trimester maternal serum chorionic gonadotropin in pregnancy with a fetus affected by homozygous alpha-thalassemia 1	Ko T.-M.; Lee T.-Y.; Chuang S.-M.; HSIAO-LIN HWA; Tseng L.-H.
臺大學術典藏	2020-02-03T08:15:28Z	Cytogenetic study of spontaneous abortions with the Giemsa banding method.	HSIAO-LIN HWA; Tseng L.H.; Ho H.N.; Ko T.M.
臺大學術典藏	2020-02-03T08:15:28Z	Prenatal diagnosis of X?linked hydrocephalus in a Chinese family with four successive affected pregnancies	Ko T.?M.; HSIAO-LIN HWA; Tseng L.?H.; Hsieh F.?J.; Huang S.?F.; Lee T.?Y.
臺大學術典藏	2020-02-03T08:15:27Z	Prenatal diagnosis by transabdominal chorionic villus sampling in the second and third trimesters	Lee T.-Y.; Chuang S.-M.; Ko T.-M.;Tseng L.-H.;Hsiao-Lin Hwa;Lee T.-Y.;Chuang S.-M.; Ko T.-M.; Tseng L.-H.; HSIAO-LIN HWA
臺大學術典藏	2020-02-03T08:15:27Z	Ultrasonographic scanning of placental thickness and the prenatal diagnosis of homozygous alpha?thalassaemia 1 in the second trimester	Chuang S.?M.; Lee T.?Y.; HSIAO-LIN HWA; Hsu P.?M.; Tseng L.?H.; Ko T.?M.;Tseng L.?H.;Hsu P.?M.;Hsiao-Lin Hwa;Lee T.?Y.;Chuang S.?M.; Ko T.?M.
臺大學術典藏	2020-02-03T08:15:26Z	Congenital adrenal hyperplasia: Molecular characterization	Ko T.-M.; Kao C.-H.; Ho H.-N.; Tseng L.-H.; HSIAO-LIN HWA; Hsu P.-M.; Chuang S.-M.; Lee T.-Y.
臺大學術典藏	2020-02-03T08:15:26Z	Molecular characterization and PCR diagnosis of Thailand deletion of α- globin gene cluster	Ko T.-M.; Tseng L.-H.; Kao C.-H.; Lin Y.-W.; HSIAO-LIN HWA; Hsu P.-M.; Li S.-F.; Chuang S.-M.
臺大學術典藏	2020-02-03T08:15:26Z	Prenatal diagnosis of monosomy 10q25 associated with single umbilical artery and sex reversal: Report of a case	Hsieh F.-J.;Shih J.-C.;Lee C.-N.;Shyu M.-K.;Tseng L.-H.;HSIAO-LIN HWA;Chung Y.-P.; Chung Y.-P.; HSIAO-LIN HWA; Tseng L.-H.; Shyu M.-K.; Lee C.-N.; Shih J.-C.; Hsieh F.-J.
臺大學術典藏	2020-02-03T08:15:25Z	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.;Hsiao-Lin Hwa;Wang T.-R.;Chuang S.- M.;Hayashi K.; Ko T.-M.; Hwu W.-L.; Lin Y.-W.; Tseng L.-H.; HSIAO-LIN HWA; Wang T.-R.; Chuang S.- M.; Hayashi K.
臺大學術典藏	2020-02-03T08:15:25Z	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.;Hsiao-Lin Hwa;Hsu P.-M.;Li S.- F.;Chuang S.-M.; Ko T.-M.; Tseng L.-H.; Kao C.-H.; Lin Y.-W.; HSIAO-LIN HWA; Hsu P.-M.; Li S.- F.; Chuang S.-M.
臺大學術典藏	2020-02-03T08:15:25Z	Second-trimester genetic amniocentesis in twin pregnancy	HSIAO-LIN HWA; Tseng L.-H.; Ko T.-M.
臺大學術典藏	2020-02-03T08:15:24Z	Molecular genetic study of Pompe disease in Chinese patients in Taiwan	Ko T.-M.; Hwu W.-L.; Lin Y.-W.; Tseng L.-H.; HSIAO-LIN HWA; Wang T.-R.; Chuang S.-M.; Ko T.-M.;Hwu W.-L.;Lin Y.-W.;Tseng L.-H.;Hsiao-Lin Hwa;Wang T.-R.;Chuang S.-M.
臺大學術典藏	2020-02-03T08:15:23Z	Prenatal diagnosis of mos46,X,del(Y)(q11.2)/45,X by cytogenetic and molecular studies with multiplex STR analysis	Hsiao-Lin Hwa;Ko T.-M.;Chang Y.-Y.;Huang C.-H.;Su Y.-N.;Tseng L.-H.;Hsieh F.-J.; HSIAO-LIN HWA; Ko T.-M.; Chang Y.-Y.; Huang C.-H.; Su Y.-N.; Tseng L.-H.; Hsieh F.-J.
臺大學術典藏	2020-02-03T08:15:17Z	Thirteen X-chromosomal short tandem repeat loci multiplex data from Taiwanese	HSIAO-LIN HWA; Chang Y.-Y.; Lee J.C.-I.; Yin H.-Y.; Chen Y.-H.; Tseng L.-H.; Su Y.-N.; Ko T.-M.
臺大學術典藏	2020-02-03T08:15:16Z	Study of the cytochrome b gene sequence in populations of Taiwan	Hsiao-Lin Hwa;Ko T.-M.;Chen Y.-C.;Chang Y.-Y.;Tseng L.-H.;Su Y.-N.;Lee J.C.-I.; HSIAO-LIN HWA; Ko T.-M.; Chen Y.-C.; Chang Y.-Y.; Tseng L.-H.; Su Y.-N.; Lee J.C.-I.
臺大學術典藏	2020-02-03T08:15:14Z	Genetic analysis of eight population groups living in Taiwan using a 13 X-chromosomal STR loci multiplex system	Ko T.-M.; Su Y.-N.; Tseng L.-H.; Chen Y.-H.; Yin H.-Y.; Hsiao-Lin Hwa;Lee J.C.-I.;Chang Y.-Y.;Yin H.-Y.;Chen Y.-H.;Tseng L.-H.;Su Y.-N.;Ko T.-M.; HSIAO-LIN HWA; Lee J.C.-I.; Chang Y.-Y.
臺大學術典藏	2020-02-03T08:15:13Z	Analysis of MTCOI and MTCYB sequence variations in eight population groups living in Taiwan	Hsiao-Lin Hwa;Lin C.-Y.;Ko T.-M.;Yin H.-Y.;Tseng L.-H.;Su Y.-N.;Lee J.C.-I.; HSIAO-LIN HWA; Lin C.-Y.; Ko T.-M.; Yin H.-Y.; Tseng L.-H.; Su Y.-N.; Lee J.C.-I.
臺大學術典藏	2020-02-03T08:15:13Z	Fourteen non-CODIS autosomal short tandem repeat loci multiplex data from Taiwanese	Hsiao-Lin Hwa;Chang Y.-Y.;Lee J.C.-I.;Yin H.-Y.;Tseng L.-H.;Su Y.-N.;Ko T.-M.; HSIAO-LIN HWA; Chang Y.-Y.; Lee J.C.-I.; Yin H.-Y.; Tseng L.-H.; Su Y.-N.; Ko T.-M.
臺大學術典藏	2020-02-03T08:15:12Z	The effectiveness of sequence variants of MTCOI and MTCYB besides entire D-loop for haplotyping in eight population groups living in Taiwan	Chen Y.-C.;Lee J.C.-I.;Lin C.-Y.;Ko T.-M.;Huang Y.-H.;Yin H.-Y.;Tseng L.-H.;Hsiao-Lin Hwa; Chen Y.-C.; Lee J.C.-I.; Lin C.-Y.; Ko T.-M.; Huang Y.-H.; Yin H.-Y.; Tseng L.-H.; HSIAO-LIN HWA
臺大學術典藏	2020-02-03T08:15:12Z	Sequence polymorphisms of mtDNA HV1, HV2 and HV3 regions in eight population groups living in Taiwan	HSIAO-LIN HWA; Ko T.-M.; Chen Y.-C.; Lin C.-Y.; Huang Y.-H.; Tseng L.-H.; Su Y.-N.; Lee J.C.-I.
臺大學術典藏	2020-02-03T08:15:10Z	Genotyping of 75 SNPs using arrays for individual identification in five population groups	HSIAO-LIN HWA; Wu L.S.H.; Lin C.-Y.; Huang T.-Y.; Yin H.-I.; Tseng L.-H.; Lee J.C.-I.
臺大學術典藏	2020-02-03T08:15:09Z	A panel of 130 autosomal single-nucleotide polymorphisms for ancestry assignment in five Asian populations and in Caucasians	Hsiao-Lin Hwa;Lin C.-P.;Huang T.-Y.;Kuo P.-H.;Hsieh W.-H.;Lin C.-Y.;Yin H.-I.;Tseng L.-H.;Lee J.C.-I.; HSIAO-LIN HWA; Lin C.-P.; Huang T.-Y.; Kuo P.-H.; Hsieh W.-H.; Lin C.-Y.; Yin H.-I.; Tseng L.-H.; Lee J.C.-I.
臺大學術典藏	2020-01-22T06:00:42Z	Prenatal detection of limb defects after chorionic villus sampling	Bor-Ching Sheu;Shyu M.?K.;Tseng L.?H.;Lin C.?J.;Hsieh F.?J.; BOR-CHING SHEU; Shyu M.?K.; Tseng L.?H.; Lin C.?J.; Hsieh F.?J.

Showing items 151-175 of 253 (11 Page(s) Totally)
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