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Showing items 71-95 of 141  (6 Page(s) Totally)
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Institution Date Title Author
臺大學術典藏 2018-09-10T07:13:33Z The spectrum of the factor 8 (F8) defects in Taiwanese patients with haemophilia A Ma, G.-C.;Chang, S.-P.;Chen, M.;Kuo, S.-J.;Chang, C.-S.;Shen, M.-C.; MING CHEN
臺大學術典藏 2018-09-10T07:13:32Z Antenatally ultrasound-impressed placenta percreta complicated with massive hemorrhage despite a combinational arterial embolization and two-stage surgery Huang, C.-C.;Chen, T.-H.;Ho, S.-Y.;Chen, M.; MING CHEN
臺大學術典藏 2018-09-10T07:13:32Z Phenotype and Genotype of Two Taiwanese Cystic Fibrosis Siblings and a Survey of Delta F508 in East Asians Lin, C.-J.;Chang, S.-P.;Ke, Y.-Y.;Chiu, H.-Y.;Tsao, L.-Y.;Chen, M.; MING CHEN
臺大學術典藏 2018-09-10T07:13:32Z Rapid prenatal confirmation of LIT1 hypomethylation using a novel quantitative method (E-Q-PCR) in fetuses with Beckwith-Wiedemann syndrome impressed with ultrasonography Ma, Gwo-Chin;Chang, Shuenn-Dyh;Chang, Yu;Chang, Shun-Ping;Yang, Chin-Wen;Lee, Ming-Jen;Lee, Tsung-Hsien;Chen, Ming; MING CHEN; MA, GWO-CHIN; CHANG, SHUENN-DYH; CHANG, YU; CHANG, SHUN-PING; YANG, CHIN-WEN; LEE, MING-JEN; LEE, TSUNG-HSIEN; CHEN, MING
臺大學術典藏 2018-09-10T07:02:24Z A recurrent ITGA9 missense mutation in human fetuses with severe chylothorax: Possible correlation with poor response to fetal therapy Ma, G.-C.;Liu, C.-S.;Chang, S.-P.;Yeh, K.-T.;Ke, Y.-Y.;Chen, T.-H.;Wang, B.B.-T.;Kuo, S.-J.;Shih, J.-C.;Chen, M.; MING CHEN; JIN-CHUNG SHIH
臺大學術典藏 2018-09-10T06:41:42Z Spinal atypical teratoid/rhabdoid tumor in a 7-year-old boy Yang, C.-S.;Jan, Y.-J.;Wang, J.;Shen, C.-C.;Chen, C.C.-C.;Chen, M.; MING CHEN
臺大學術典藏 2018-09-10T06:41:41Z Cytogenetic analysis of the Formosan pangolin, Manis pentadactyla pentadactyla (Mammalia: Pholidota) Wu, S.-H.;Chen, M.;Chin, S.-C.;Lee, D.-J.;Wen, P.-Y.;Chen, L.-W.;Wang, B.-T.;Yu, H.-T.; MING CHEN
臺大學術典藏 2018-09-10T06:41:41Z Delineation of an isodicentric Y chromosome in a mosaic 45,X/46,X,idic(Y)(qter-p11.3 Wu, H.-H.;Lee, T.-H.;Chen, C.-D.;Yeh, K.-T.;Chen, M.Wu, Hh;Lee, Th;Chen, Cd;Yu, Ht;Yeh, Kt;Chen, M; Wu, HH;Lee, TH;Chen, CD;Yu, HT;Yeh, KT;Chen, M; MING CHEN; Wu, HH; Lee, TH; Chen, CD; Yu, HT; Yeh, KT; Chen, M
臺大學術典藏 2018-09-10T06:41:41Z Diagnostic confirmation of X-linked recessive ichthyosis by fluorescent in situ hybridization - A case report Ho, C.-Y.;Yang, K.-C.;Chen, M.;Chang, S.-P.;Yin, P.-L.; MING CHEN
臺大學術典藏 2018-09-10T06:41:41Z First prenatal exclusion of cystic fibrosis in East Asia Wong, L.-J.C.;Lee, M.-H.;Chen, M.;Alper, O.M.;Tsao, L.-Y.;Wang, B.-T.; MING CHEN
臺大學術典藏 2018-09-10T06:41:41Z Interstitial deletion 13q31 associated with normal phenotype: Cytogenetic study of a family with concomitant segregation of reciprocal translocation and interstitial deletion Ke, Y.-Y.;Lee, D.-J.;Ma, G.-C.;Lee, M.-H.;Wang, B.-T.;Chen, M.; MING CHEN
臺大學術典藏 2018-09-10T06:41:41Z Mutation analysis of TSC gene in tuberous sclerosis complex patient - Case report Ho, C.-Y.;Yang, K.-C.;Chen, M.;Chang, S.-P.; MING CHEN
臺大學術典藏 2018-09-10T06:41:40Z Balloon pulmonary valvuloplasty for valvular pulmonary stenosis in double outlet right ventricle incriminating 46,X,der(X)t(X;3)(q28;q13.2)mat in an infant Lee, M.-L.;Chen, M.;Lee, M.-H.; MING CHEN
臺大學術典藏 2018-09-10T06:41:40Z Comparison of immunohistochemical and fluorescence in situ hybridization assessment for HER-2/neu status in Taiwanese breast cancer patients Kuo, S.-J.;Wang, B.B.-T.;Chang, C.-S.;Chen, T.-H.;Yeh, K.-T.;Lee, D.-J.;Yin, P.-L.;Chen, M.; MING CHEN
臺大學術典藏 2018-09-10T06:06:48Z Prenatal sonographic features of hypospadia: Two- and three-dimensional findings Fang, K.-H.;Wu, J.-L.;Chen, M.;Yeh, G.-P.;Chou, P.-H.;Hsu, J.-C.;Hsieh, C.T.-C.; MING CHEN
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 2018-09-10T06:06:47Z Huge duplication cyst of small intestine: Ultrasonographic features and prenatal aspiration [2] Chen, M.;Ho, W.-K.;Hsieh, T.-C.;Lee, C.-S.;Hsiao, C.-C.;Chang, S.-P.;Lee, D.-J.;Yang, A.D.; MING CHEN
臺大學術典藏 2018-09-10T06:06:47Z Prenatal identification of small supernumerary marker chromosomes by FISH in an infant born with mild congenital anomalies [8] Chen, M.;Chang, S.-P.;Yin, P.-L.;Sapeta, M.;Barringer, S.;Kuo, S.-J.;Yu, H.-T.;Wang, B.B.-T.; MING CHEN
臺大學術典藏 2018-09-10T06:05:38Z Persistent fifth aortic arch associated with 22q11.2 deletion syndrome Lee, M.-L.;Chen, H.-N.;Chen, M.;Tsao, L.-Y.;Wang, B.-T.;Lee, M.-H.;Chiu, I.-S.; MING CHEN; ING-SH CHIU
臺大學術典藏 2018-09-10T05:32:43Z Management of oligohydramnios with antepartum amnioinfusion, amniopatch and cerclage Chen, M.;Hsieh, C.-Y.;Cameron, A.D.;Shih, J.-C.;Lee, C.-N.;Ho, H.-N.;Chen, T.-H.;Chen, C.-P.; MING CHEN; HONG-NERNG HO; CHIEN-NAN LEE
臺大學術典藏 2018-09-10T05:22:14Z Fetal OK-432 pleurodesis: Complete or incomplete? [2] Chen, M.;Shih, J.C.;Wang, B.T.;Chen, C.P.;Yu, C.L.; MING CHEN; JIN-CHUNG SHIH
臺大學術典藏 2018-09-10T05:03:35Z Meconium peritonitis presenting as isolated massive fetal ascites [6] Chen, F.-Y. and Chen, M. and Shih, J.-C. and Tsao, P.-N. and Lee, C.-N. and Hsieh, F.-J.; MING CHEN; CHIEN-NAN LEE; JIN-CHUNG SHIH; PO-NIEN TSAO
臺大學術典藏 2018-09-10T05:03:08Z Redundant skin over the nape in a girl with monosomy 1p36 caused by a de-novo satellited derivative chromosome: A possible new feature? Wang, B.T.;Chen, M.; MING CHEN
臺大學術典藏 2018-09-10T05:03:08Z Trisomy 13 mosaicism: Study of serial cytogenetic changes in a case from early pregnancy to infancy Chen, M.;Yeh, G.-P.;Shih, J.-C.;Wang, B.-T.; MING CHEN; JIN-CHUNG SHIH
臺大學術典藏 2018-09-10T05:03:07Z Early-Onset Oligohydramnios Complicated with Hypertension, Hyperthyroidism and Coexisting Elevated Urine Vanillylmandelic Acid of Unknown Origin, Mimicking a Pheochromocytoma Wu, J.-L.;Chen, M.;Hsieh, T.-C.;Chen, T.-H.;Chou, P.-H.;Lin, K.-C.; MING CHEN

Showing items 71-95 of 141  (6 Page(s) Totally)
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