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Showing items 76-125 of 141  (3 Page(s) Totally)
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Institution Date Title Author
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
臺大學術典藏 2018-09-10T05:03:07Z Invasive Fetal Therapy: Global Status and Local Development Chen, M.;Chen, C.-P.; MING CHEN
臺大學術典藏 2018-09-10T05:03:07Z Prenatal diagnosis of a fetus affected with down syndrome and deletion 1p36 syndrome by fluorescence in situ hybridization and spectral karyotyping Hsieh, L.-J.;Hsieh, T.-C.;Yeh, G.-P.;Lin, M.-I.;Chen, M.;Wang, B.B.-T.; MING CHEN
臺大學術典藏 2018-09-10T04:44:00Z Effect of conjugated equine estrogen in combination with two different progestogens on the risk factors of coronary heart disease in postmenopausal Chinese women in Taiwan: A randomized one-year study Chang, T.-C.;Lien, Y.-R.;Chen, M.;Cheng, S.-P.;Chen, R.-J.;Chow, S.-N.; RUEY-JIEN CHEN; MING CHEN; YIH-RON LIEN
臺大學術典藏 2018-09-10T04:38:18Z Simultaneous occurrence of hepatic focal nodular hyperplasia and uterine endometrial stromal nodule in a patient having treated breast infiltrating ductal carcinoma Chen, C.-A.;Chen, M.; MING CHEN; CHI-AN CHEN
臺大學術典藏 2018-09-10T04:32:16Z Trisomy 13 manifested as hypoplastic left heart and other structural abnormalities [5] Chen, M.;Shih, J.-C.;Wang, B.-T.; MING CHEN; JIN-CHUNG SHIH
臺大學術典藏 2018-09-10T04:32:10Z Comparison of the difference in histopathology and cell cycle kinetics among the postmenopausal endometrium treated with different progestins in sequential-combined hormone replacement therapy Chang, T.-C.;Chen, M.;Lien, Y.-R.;Chen, R.-J.;Chow, S.-N.; MING CHEN; YIH-RON LIEN
臺大學術典藏 2018-09-10T03:52:47Z Additive effect of alfacalcidol on bone mineral density of the lumbar spine in Taiwanese postmenopausal women treated with hormone replacement therapy and calcium supplementation: A randomized 2-year study Chen, M.;Chow, S.-N.; MING CHEN
臺大學術典藏 2018-09-10T03:41:52Z Cell cycle analysis and detection of proliferative cell nuclear antigen of the endometrium after hormone replacement therapy Chow, S.-N.;Chen, M.;Chen, P.-J.;Chen, R.-J.;Chien, C.-H.; RUEY-JIEN CHEN; MING CHEN
臺大學術典藏 2018-09-10T03:32:34Z Tuboovarian abscess mimicking malignancy: Report of two cases Chow, S.-N.;Chen, M.; MING CHEN
義守大學 2015-11 Thermolability, enzymatic degradation and aminolysis of solution-grown single crystals of novel poly(ethylene succinate-co-5mol% trimethylene succinate)s Wen-Chuan Hsieh;Guan-Cheng Chen;Chun-Che Sung;Ken-Ichi Kasuya;Yuya Tachibana;Chi-he Chen;Ming Chen;Tzong-Rong Ling;Chih-Pong Chang
中國醫藥大學 2015-08 Prescription patterns of Chinese herbal products for patients with sleep disorder and major depressive disorder in Taiwan 陳懿琳(Yi-Lin Chen);李建瑩(Chien-Ying Lee)*;黃光華(Kuang-Hua Huang);(Yu-Hsiang Kuan);(Ming Chen)*
亞洲大學 2014-03 Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 15 Chih-Ping Chen;Ming Chen;Yi-Ning Su;Schu-Rern Chern; Peih-Shan Wu;Shun-Ping Chang;Yu-Ling Kuo;Wen-Lin Chen;Wayseen Wang
中國醫藥大學 2014-03 Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 15 陳持平(Chih-Ping Chen)*;(Ming Chen);(Yi-Ning Su);(Schu-Rern Chern);(Peih-Shan Wu);(Shun-Ping Chang);(Yu-Ling Kuo);(Wen-Lin Chen);(Wayseen Wang)
亞洲大學 2014-02 Prenatal diagnosis and molecular cytogenetic characterization of de novo pure partial trisomy 6p associated with microcephaly, craniosynostosis and abnormal maternal serum biochemistry Chih-Ping Chen;Ming Chen;Chen-Yu Chen;Schu-Rern Chern;Peih-Shan Wu;Shun-Ping Chang;Yu-Ling Kuo;Wen-Lin Chen;Chen-Wen Pan;Wayseen Wang
臺大學術典藏 2014 Two Y chromosomes with duplication of the distal long arm including the entire AZFc region Hsu, H.-K.;Su, M.-T.;Chen, M.;Yen, P.;Kuo, P.-L.; MING CHEN
中國醫藥大學 2013-01 Array comparative genomic hybridization characterization of prenatally detected de novo apparently balanced reciprocal translocations with or without genomic imbalance in other chromosome 陳持平(Chih-Ping Chen)*;(Ming Chen);(Gwo-Chin Ma);(Yi-Ning Su);(Tsang-Ming Ko);(Yi-Hui Lin);(Wayseen Wang)
中國醫藥大學 2012-09 Rapid positive confirmation of mosaicism for a small supernumerary marker chromosome as r(8) by interphase FISH, QF-PCR and aCGH on uncultured amniocytes in a pregnancy with fetal pyelectasis 陳持平(Chih-Ping Chen)*;(Shuenn-Dyh Chang);(Yi-Ning Su);(Ming Chen);(Schu-Rern Chern);(Jun-Wei Su);(Yu-Ting Chen);(Wen-Lin Chen,);(Chen-Wen Pan);(Meng-Shan Lee);(Wayseen Wang)
中國醫藥大學 2012-09 Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 2 陳持平(Chih-Ping Chen)*;(Ming Chen);(Schu-Rern Chern);(Peih-Shan Wu);(Shun-Ping Chang);(Dong-Jay Lee);(Yu-Ting Chen);(Li-Feng Chen);(Jun-Wei Su,);(Alan Hwa-Ruey Hsieh);(Alex Hwa-Jiun Hsieh);(Wayseen Wang)
中國醫藥大學 2012-06 Inv dup del(10q): Identification by fluorescence in situ hybridization and array comparative genomic hybridization in a fetus with two concurrent chromosomal rearrangements 陳持平(Chih-Ping Chen)*;(Ming Chen);(Yi-Ning Su);(Jian-Pei Huang);(Gwo-Chin Ma);(Shun-Ping Chang);(Schu-Rern Chern);(Yu-Ting Chen);(Jun-Wei Su);(Chen-Chi Lee);(Dai-Dyi Town);(Wayseen Wang)
中國醫藥大學 2012-03 Unexplained shortening of the long bones in the third trimester as the only prenatal feature in a male fetus with 45,X/46,X,r(Y) mosaicism 陳持平(Chih-Ping Chen)*;(Yi-Ning Su);(Ming Chen);蔡輔仁(Fuu-Jen Tsai);(Yi-Yung Chen);(Gwo-Chin Ma);(Shun-Ping Chang);(Jun-Wei Su);(Yu-Ting Chen);(Wen-Lin Chen);(Li-Feng Chen);(Wayseen Wang)
中國醫藥大學 2011-12 A de novo duplication of chromosome 21q22.11->qter associated with Down syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings 陳持平(Chih-Ping Chen)*;(Hsu-Kuaing Huang);(Pei-Ying Lin);(Yi-Ning Su);(Ming Chen);蔡輔仁(Fuu-Jen Tsai);(Pei-Chen Wu);(Schu-Rern Chern);(Yu-Ting Chen);(Chen-Chi Lee);(Wayseen Wang)
中國醫藥大學 2011-12 A 20.5-Mb germline deletion of 13q13.1->q14.3 and somatic mutations of the RB1 gene in an 8-year-old girl with unilateral retinoblastoma, developmental delay and mental retardation 陳持平(Chih-Ping Chen)*;(Ling-Yuh Kao);(Yi-Ning Su);(Ming Chen);(Shueen-Dyh Chang);(Wayseen Wang)
中國醫藥大學 2011-09 Mosaic supernumerary r(1)(p13.2q23.3) in a 10-year-old girl with epilepsy, facial asymmetry, psychomotor retardation, kyphoscoliosis, dermatofibrosarcoma and multiple exostoses 陳持平(Chih-Ping Chen)*;(Shuan-Pei Lin);(Ming Chen);(Yi-Ning Su);(Schu-Rern Chern);(Tao-Yeuan Wang);(Yu-Peng Liu);蔡輔仁(Fuu-Jen Tsai);(Chen-Chi Lee);(Yen-Jiun Chen);(Wayseen Wang)
中國醫藥大學 2011-09 Prenatal diagnosis of mosaic trisomy 8: clinical report and literature review 陳持平(Chih-Ping Chen)*;(Ming Chen);(Yi-Ju Pan);(Yi-Ning Su);(Schu-Rern Chern);蔡輔仁(Fuu-Jen Tsai);(Yu-Ting Chen);(Wayseen Wang)
中國醫藥大學 2011-09 Prenatal diagnosis and molecular cytogenetic characterization of a mosaic derivative Y chromosome derived from a de novo unbalanced reciprocal Yq;13q translocation 陳持平(Chih-Ping Chen)*;(Yi-Ning Su);(Ming Chen);(Jain-Pei Huang);蔡輔仁(Fuu-Jen Tsai);(Pei-Chen Wu);(Wen-Lin Chen);(Wayseen Wang)
中國醫藥大學 2010-12 Chromosome 1p36 deletion syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings 陳持平(Chih-Ping Chen)*; (Ming Chen); (Yi-Ning Su); (Chin-Yuan Hsu); 蔡輔仁(Fuu-Jen Tsai); (Schu-Rern Chern); (Pei-Chen Wu); (Chen-Chi Lee); (Wayseen Wang)
中國醫藥大學 2010-12 Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 8 陳持平(Chih-Ping Chen)*; (Ming Chen); (Tsang-Ming Ko); (Gwo-Chin Ma); 蔡輔仁(Fuu-Jen Tsai); (Ming-Song Tsai); (Pei-Chen Wu); (Chen-Chi Lee); (Li-Feng Che); (Wayseen Wang)
中國醫藥大學 2010-09 Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 7p (7p15.3->pter) and partial monosomy 13q (13q33.3->qter) associated with Dandy-Walker malformation, abnormal skull development and microcephaly 陳持平(Chih-Ping Chen)*; (Ming Chen); (Yi-Ning Su); 蔡輔仁(Fuu-Jen Tsai); (Schu-Rern Chern); (Chin-Yuan Hsu); (Pei-Chen Wu); (Dai-Dyi Town); (Dong-Jay Lee); (Gwo-Chin Ma); (Wayseen Wang)
亞洲大學 2010-03 Ventriculomegaly, intrauterine growth restriction and congenital heart defects as salient prenatal sonographic findings of Miller-Dieker lissencephaly syndrome associated with monosomy 17p (17p13.2->pter) in a fetus Chih-Ping Chen;Yu-Peng Liu;Shaun-Pei Lin;Ming Chen;Fuu-Jen Tsai;Yu-Ting Chen;Li-Feng Chen;Jonathan Kwei Hwang;Wayseen Wang
中國醫藥大學 2010-03 Ventriculomegaly, intrauterine growth restriction and congenital heart defects as salient prenatal sonographic findings of Miller-Dieker lissencephaly syndrome associated with monosomy 17p (17p13.2->pter) in a fetus 陳持平(Chih-Ping Chen)*; (Yu-Peng Liu); (Shuan-Pei Lin); (Ming Chen); 蔡輔仁(Fuu-Jen Tsai); (Yu-Ting Chen); (Li-Feng Chen); (Jonathan Kwei Hwang); (Wayseen Wang)

Showing items 76-125 of 141  (3 Page(s) Totally)
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