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显示项目 683011-683060 / 2349128 (共46983页)
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机构 日期 题名 作者
亞洲大學 2012-03 Prenatal diagnosis of mosaic ring chromosome 15 with abnormal maternal serum Down syndrome screening and Dandy- Walker malformation 陳持平;Chen, Chih-Ping
中國醫藥大學 2007-05 Prenatal diagnosis of mosaic ring chromosome 4 陳持平(Chih-Ping Chen)*; 徐金源(Chin-Yuan Hsu); 曾嶔元(Chin-Yuan Tzen); 李貞姬(Chen-Chi Lee); 陳文玲(Wen-Lin Chen); 陳麗鳳(Li-Feng Chen); 王偉信(Wayseen Wang)
亞洲大學 2016-06 Prenatal diagnosis of mosaic small supernumerary marker chromosome 17 associated with ventricular septal defect, developmental delay and speech delay Chen)*, 陳持平(Chih-Ping;Chiang), Sheng Chiang(Sheng;Wang), Kung-Liahng(Kung-Liahng;Cho), Fu-Nan Cho(Fu-Nan;Chen), Ming Chen(Ming;Chern), Schu-Rern Ch(Schu-Rern;Wu), Peih-Shan Wu(Peih-Shan;Chen), Yen-Ni Chen(Yen-Ni;(Shin-Wen Chen,);(Shun-Ping Chang,);Chen), Weu-Lin Chen(Weu-Lin;Wang), Wayseen Wang(Wayseen
亞洲大學 2016-06 Prenatal diagnosis of mosaic small supernumerary marker chromosome 17 associated with ventricular septal defect, developmental delay and speech delay 陳持平;Chen, Chih-Ping;*;Chiang, Sheng;Chiang, Sheng;Kung-Liahng;Wang, Kung-Liahng;Cho, Fu-Nan;Cho, Fu-Nan;Chen, Ming;Chen, Ming;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Chen, Yen-Ni;Chen, Yen-Ni;Shin-Wen Chen;Shun-Ping Chang;Chen, Weu-Lin;Chen, Weu-Lin;Wang, Wayseen;Wang, Wayseen
亞洲大學 2016-06 Prenatal diagnosis of mosaic small supernumerary marker chromosome 17 associated with ventricular septal defect, developmental delay and speech delay 陳持平;Chih-Ping Chen;*;Sheng Chiang;Sheng Chiang;Kung-Liahng;Kung-Liahng Wang;Fu-Nan Cho;Fu-Nan Cho;Ming Chen;Ming Chen;Schu-Rern Ch;Schu-Rern Chern;Peih-Shan Wu;Peih-Shan Wu;Yen-Ni Chen;Yen-Ni Chen;, ;Shin-Wen Chen,;,;Shun-Ping Chang,;Weu-Lin Chen;Weu-Lin Chen;Wayseen Wang;Wayseen Wang;;
臺大學術典藏 2018-09-10T15:38:52Z Prenatal diagnosis of mosaic small supernumerary marker chromosome 17 associated with ventricular septal defect, developmental delay, and speech delay Chen, C.-P.;Chiang, S.;Wang, K.-L.;Cho, F.-N.;Chen, M.;Chern, S.-R.;Wu, P.-S.;Chen, Y.-N.;Chen, S.-W.;Chang, S.-P.;Chen, W.-L.;Wang, W.; MING CHEN
中國醫藥大學 2003 Prenatal diagnosis of mosaic tetrasomy 10p associated with megacisterna magna, echogenic focus of left ventricle, umbilical cord cysts and distal arthrogryposis Wu, YC; Yu, MT; Chen, LC; Chen, CL; Yang, ML
中國醫藥大學 2012-12 Prenatal diagnosis of mosaic tetrasomy 18p 陳持平(Chih-Ping Chen)*;(Tsang-Ming Ko);(Yi-Ning Su);(Schu-Rern Chern);(Jun-Wei Su);(Yu-Ting Chen);(Dai-Dyi Town);(Wayseen Wang)
亞洲大學 201309 Prenatal diagnosis of mosaic trisomy 12 associated with congenital overgrowth 陳持平;Chen, Chih-Ping;Ch, Shing-Jyh;Chang, Shing-Jyh;Su, Jun-Wei;Su, Jun-Wei;Chen, Yu-Ting;Chen, Yu-Ting;Wang, Wayseen;Wang, Wayseen
國立臺灣大學 2004 Prenatal Diagnosis of Mosaic Trisomy 16 Associated with Congenital Diaphragmatic Hernia and Elevated Maternal Serum Alpha-Fetoprotein and Human Chorionic Gonadotrophin 陳持平; 施景中; 陳樹人; 李貞姬; 王偉信; CHEN, CHIH-PING; SHIH, JIN-CHUNG; CHERN, SCHU-RERN; LEE, CHEN-CHI; WANG, WAYSEEN
臺大學術典藏 2021-02-04T06:46:55Z Prenatal diagnosis of mosaic trisomy 16 associated with congenital diaphragmatic hernia and elevated maternal serum alpha-fetoprotein and human chorionic gonadotrophin Chen C.-P.;Jin-Chung Shih;Chern S.-R.;Lee C.-C.;Wang W.; Chen C.-P.; JIN-CHUNG SHIH; Chern S.-R.; Lee C.-C.; Wang W.
亞洲大學 201309 Prenatal diagnosis of mosaic trisomy 2 associated with abnormal maternal serum screening, oligohydramnios, intrauterine growth restriction, ventricular septal defect, preaxial polydactyly and facial dysmorphism 陳持平;Chen, Chih-Ping;Chen, Yi-Yung;Chen, Yi-Yung;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Su, Jun-Wei;Su, Jun-Wei;Chen, Yu-Ting;Chen, Yu-Ting;Lee, Chen-Chi;Lee, Chen-Chi;Chen, Li-Feng;Li-Feng Chen, ;Wang, Wayseen;Wang, Wayseen
亞洲大學 2011-09 Prenatal diagnosis of mosaic trisomy 2: discrepancy between molecular cytogenetic analyses of uncultured amniocytes and karyotyping of cultured amniocytes in a pregnancy with severe fetal intrauterine growth restriction 陳持平;Chen, Chih-Ping
中國醫藥大學 2011-09 Prenatal diagnosis of mosaic trisomy 2: discrepancy between molecular cytogenetic analyses of uncultured amniocytes and karyotyping of cultured amniocytes in a pregnancy with severe fetal intrauterine growth restriction 陳持平(Chih-Ping Chen)*;(Yi-Ning Su);(Shin-Yu Lin);(Schu-Rern Chern);(Yu-Ting Chen);(Meng-Shan Lee);(Wayseen Wang)
臺大學術典藏 2020-02-10T06:49:21Z Prenatal diagnosis of mosaic trisomy 2: Discrepancy between molecular cytogenetic analyses of uncultured amniocytes and karyotyping of cultured amniocytes in a pregnancy with severe fetal intrauterine growth restriction Chen C.-P;Su Y.-N;Shin-Yu Lin;Chern S.-R;Chen Y.-T;Lee M.-S;Wang W.; Chen C.-P; Su Y.-N; SHIN-YU LIN; Chern S.-R; Chen Y.-T; Lee M.-S; Wang W.
亞洲大學 2020-01-20 Prenatal diagnosis of mosaic trisomy 8 by amniocentesis in a fetus with ventriculomegaly and dysgenesis of the corpus callosum Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Che, Shin-Wen; Chen, Shin-Wen; Wang, Wayseen; Ch, Chih-Ping; Chen, Chih-Ping; Hs, Chin-Yuan; Hsu, Chin-Yuan
亞洲大學 2011-09 Prenatal diagnosis of mosaic trisomy 8: clinical report and literature review 陳持平;Chen, Chih-Ping
國立臺灣大學 2011 Prenatal Diagnosis of Mosaic Trisomy 8: Clinical Report and Literature Review 陳持平; 陳明; 潘怡如; 蘇怡寧; 陳樹人; 蔡輔仁; 王偉信; CHEN, CHIH-PING; CHEN, MING; PAN, YI-JU; SU, YI-NING; CHERN, SCHU-RERN; TSAI, FUU-JEN; WANG, WAYSEEN
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)
臺大學術典藏 2018-09-10T08:50:12Z Prenatal diagnosis of mosaic trisomy 8: Clinical report and literature review Chen, Y.-T.;Wang, W.;Chen, Chih-Ping;Chen, Ming;Pan, Yi-Ju;Su, Yi-Ning;Chern, Schu-Rern;Tsai, Fuu-Jen;Wang, Wayseen; CHEN, CHIH-PING;CHEN, MING;PAN, YI-JU;SU, YI-NING;CHERN, SCHU-RERN;TSAI, FUU-JEN;WANG, WAYSEEN; 陳持平;陳明;潘怡如;蘇怡寧;陳樹人;蔡輔仁;王偉信; MING CHEN; CHEN, CHIH-PING; CHEN, MING; PAN, YI-JU; SU, YI-NING; CHERN, SCHU-RERN; TSAI, FUU-JEN; WANG, WAYSEEN
亞洲大學 2011-12 Prenatal diagnosis of mosaic trisomy 9 陳持平;Chen, Chih-Ping
亞洲大學 2017-04 Prenatal diagnosis of mosaicism for trisomy 15 in a single colony at amniocentesis with a favorable fetal outcome Wang, 陳持平;Chih-Ping Chen;Fang-Yu Hung;Fang-Yu Hung;Schu-Rern Ch;Schu-Rern Chern;Peih-Shan Wu;Peih-Shan Wu;Yen-Ni Chen;Yen-Ni Chen;Shin-Wen Che;Shin-Wen Chen;Chien-Wen Ya;Chien-Wen Yang;Wen-Lin Chen;Wen-Lin Chen;Wayseen Wang;Wayseen
亞洲大學 2017-08 Prenatal diagnosis of mosaicism for trisomy 2 in a single colony at amniocentesis in a pregnancy with a favorable outcome Wang, 陳持平;Chih-Ping Chen;Jian-Pei Hua;Jian-Pei Huang;Schu-Rern Ch;Schu-Rern Chern;Shin-Wen Che;Shin-Wen Chen;Shih-Ting La;Shih-Ting Lai;Peih-Shan Wu;Peih-Shan Wu;Chen-Chi Lee;Chen-Chi Lee;Chien-Wen Ya;Chien-Wen Yang;Wayseen Wang;Wayseen
亞洲大學 2019-11 Prenatal diagnosis of mosaicism for trisomy 7 in a single colony at amniocentesis in a pregnancy with a favorable outcome 陳持平;Chen, Chih-Ping;Hung, Fang-Yu;Hung, Fang-Yu;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Che, Shin-Wen;Chen, Shin-Wen;Wu, Fang-Tzu;Wu, Fang-Tzu;Town, Dai-Dyi;Town, Dai-Dyi;Wang, Wayseen;Wang, Wayseen
國立成功大學 2003-09 Prenatal diagnosis of occipital meningocele using three-dimensional ultrasonography Chen, Sheng-Hsien; Chang, Fong-Ming
中國醫藥大學 2001 Prenatal diagnosis of oculocutaneous albinism two mutations located at the same allele Hsieh, YY; Wu, JY; Chang, CC; Tsai, FJ; Lee, CC; Tsai, HD; Tsai, CH
中國醫藥大學 2001 Prenatal diagnosis of oculocutaneous albinism two mutations located at the same allele Hsieh, YY; Wu, JY; Chang, CC; Tsai, FJ; Lee, CC; Tsai, HD; Tsai, CH
國立成功大學 1998-05 Prenatal diagnosis of otocephaly using two-dimensional and three-dimensional ultrasonography Lin, H. H.; Liang, R. I.; Chang, Fong-Ming; Chang, C. H.; Yu, C. H.; Yang, H. B.
亞洲大學 2010-12 Prenatal diagnosis of partial monosomy 1q (1q42.3->qter) associated with hydrocephalus and corpus callosum agenesis 陳持平;Chen, Chih-Ping;Chern, Schu-Rern;Tsai, Fuu-Jen;Lin, Hung-Hung;Wu, Pei-Chen;Lee, Chen-Chi;Pan, Chen-Wen;Wang, Wayseen
中國醫藥大學 2010-12 Prenatal diagnosis of partial monosomy 1q (1q42.3->qter) associated with hydrocephalus and corpus callosum agenesis 陳持平(Chih-Ping Chen)*; (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Hung-Hung Lin); (Pei-Chen Wu); (Chen-Chi Lee); (Chen-Wen Pan); (Wayseen Wang)
亞洲大學 2016-08 Prenatal diagnosis of partial monosomy 5p (5p15.1->pter) and partial trisomy 7p (7p15.2->pter) associated with cystic hygroma, abnormal skull development and ventriculomegaly Wang;, 陳持平;Chih-Ping Chen;*;Liang-Kai Wa;Liang-Kai Wang;Schu-Rern Ch;Schu-Rern Chern;Peih-Shan Wu;Peih-Shan Wu;Kevin Ko;Kevin Ko;Yen-Ni Chen;Yen-Ni Chen;Shin-Wen Che;Shin-Wen Chen;Meng-Shan Le;Meng-Shan Lee;Wayseen Wang;Wayseen
亞洲大學 2016-08 Prenatal diagnosis of partial monosomy 5p (5p15.1->pter) and partial trisomy 7p (7p15.2->pter) associated with cystic hygroma, abnormal skull development and ventriculomegaly 陳持平;Chen, Chih-Ping;*;Wa, Liang-Kai;Wang, Liang-Kai;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Ko, Kevin;Ko, Kevin;Chen, Yen-Ni;Chen, Yen-Ni;Che, Shin-Wen;Chen, Shin-Wen;Le, Meng-Shan;Lee, Meng-Shan;Wang, Wayseen;Wang, Wayseen
中國醫藥大學 2005 Prenatal diagnosis of partial trisomy 10q (10q25.3 -> qter) and partial monosomy 18q (18q23 -> qter) Chen, CP; Chern, SR; Chang, TY; Lee, CC; Chen, WL; Wang, W
亞洲大學 2009 PRENATAL DIAGNOSIS OF PARTIAL TRISOMY 14q (14q31.1 -> qter) AND PARTIAL MONOSOMY 5p (5p13.2 -> pter) ASSOCIATED WITH POLYHYDRAMNIOS, SHORT LIMBS, MICROPENIS AND BRAIN MALFORMATIONS Chen, CP (Chen, C-P); Chern, SR (Chern, S. -R.); Tsai, FJ (Tsai, F-J.); Lee, CC (Lee, C. -C.); Chen, LE (Chen, L. -E); Wang, W (Wang, W.)
亞洲大學 2012-03 Prenatal diagnosis of partial trisomy 16p (16p12.2->pter) and partial monosomy 22q (22q13.31->qter) associated with increased nuchal translucency and abnormal maternal serum biochemistry in the first trimester 陳持平;Chen, Chih-Ping
中國醫藥大學 2012-03 Prenatal diagnosis of partial trisomy 16p (16p12.2->pter) and partial monosomy 22q (22q13.31->qter) associated with increased nuchal translucency and abnormal maternal serum biochemistry in the first trimester 陳持平(Chih-Ping Chen)*;(Tsang-Ming Ko);(Yi-Ning Su);(Chin-Yuan Hsu);(Yi-Yung Chen);(Jun-Wei Su);(Wen-Lin Chen);(Wayseen Wang)
中國醫藥大學 2005 Prenatal diagnosis of partial trisomy 16q and distal 22q13 deletion associated with dolichocephaly and frontal bossing on second-trimester ultrasound Chen, CP; Hsu, CY; Huang, JK; Lee, CC; Chen, WL; Wang, W
亞洲大學 2008-10 Prenatal Diagnosis of Partial Trisomy 3p (3p21 -> pter) and Partial Monosomy 11q (11q23 -> qter) Associated with Abnormal Sonographic Findings of Holoprosencephaly, Orofacial Clefts, Pyelectasis and a Unilateral Duplex Renal System Chen, CP (Chen, Chih-Ping); Wang, TH (Wang, Tzu-Hao); Lin, CC (Lin, Chyi-Chyang); Tsai, FJ (Tsai, Fuu-Jen); Hsieh, LJ (Hsieh, Lie-Jiau); Wang, W (Wang, Wayseen)
亞洲大學 2008-10 Prenatal Diagnosis of Partial Trisomy 3p (3p21 -> pter) and Partial Monosomy 11q (11q23 -> qter) Associated with Abnormal Sonographic Findings of Holoprosencephaly, Orofacial Clefts, Pyelectasis and a Unilateral Duplex Renal System 陳持平;Chen, Chih-Ping;Wang, Tzu-Hao;Lin, Chyi-Chyang;Tsai, Fuu-Jen;Hsieh, Lie-Jiau;Wang, Wayseen
中國醫藥大學 2008-10 Prenatal diagnosis of partial trisomy 3p (3p21->pter) and partial monosomy 11q (11q23->qter) associated with abnormal sonographic findings of alobar holoprosencephaly, orofacial clefts, pyelectasis and a unilateral duplex renal system 陳持平(Chih-Ping Chen)*; (Tzu-Hao Wang); (Chin-Yuan Hsu); (Chin-Yuan Tzen); (Chen-Chi. Lee); (Wayseen Wang)
亞洲大學 2013-03 Prenatal diagnosis of partial trisomy 3q (3q27.3->qter) and partial monosomy 14q (14q31.3->qter) of paternal origin associated with fetal hypotonia, arthrogryposis, scoliosis and hyperextensible joints 陳持平;Chen, Chih-Ping;Cha, Yao-Lung;Chang, Yao-Lung;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Su, Jun-Wei;Su, Jun-Wei;Chen, Wen-Lin;Chen, Wen-Lin;Chen, Li-Feng;Chen, Li-Feng;Wang, Wayseen;Wang, Wayseen
中國醫藥大學 2013-03 Prenatal diagnosis of partial trisomy 3q (3q27.3->qter) and partial monosomy 14q (14q31.3->qter) of paternal origin associated with fetal hypotonia, arthrogryposis, scoliosis and hyperextensible joints 陳持平(Chih-Ping Chen)*;(Yao-Lung Chang);(Schu-Rern Chern);(Peih-Shan Wu);(Jun-Wei Su);(Wen-Lin Chen);(Li-Feng Chen);(Wayseen Wang)
臺大學術典藏 2020-02-12T04:05:35Z Prenatal diagnosis of paternal uniparental disomy for chromosome 14 using a single-nucleotide-polymorphism-based microarray analysis: A case report Lin S.-Y.;Tai Y.-Y;Hsu W.-W;Lin M.-W;CHIEN-NAN LEE;Chen C.-L; Chen C.-L; CHIEN-NAN LEE; Lin M.-W; Hsu W.-W; Tai Y.-Y; Lin S.-Y.
臺大學術典藏 2020-05-24T05:47:52Z Prenatal diagnosis of paternal uniparental disomy for chromosome 14 using a single-nucleotide-polymorphism-based microarray analysis: A case report Chen C.-L.; Lee C.-N.; MING-WEI LIN; Hsu W.-W.; Tai Y.-Y.; Lin S.-Y.
臺大學術典藏 2021-02-04T06:04:28Z Prenatal diagnosis of paternal uniparental disomy for chromosome 14 using a single-nucleotide-polymorphism-based microarray analysis: A case report Chen C.-L.;Chien-Nan Lee;Lin M.-W.;Hsu W.-W.;Tai Y.-Y.;Lin S.-Y.; Chen C.-L.; CHIEN-NAN LEE; Lin M.-W.; Hsu W.-W.; Tai Y.-Y.; Lin S.-Y.
國立成功大學 2013-03 Prenatal diagnosis of pentalogy of Cantrell using three-dimensional ultrasound Yang, Ting-Yu; Tsai, Pei-Yin; Cheng, Yueh-Chin; Chang, Fong-Ming; Chang, Chiung-Hsin
亞洲大學 2010-09 Prenatal diagnosis of persistent cloaca with hydrometrocolpos and ascites by magnetic resonance imaging in one fetus of a dizygotic twin pregnancy 陳持平;Chen, Chih-Ping;Liu, Yu-Peng;Chang, Tung-Yao;Tsai, Fuu-Jen;Chen, Chen-Yu;Wu, Pei-Chen;Chen, Teresa Hsiao-Tien;Wang, Wayseen
中國醫藥大學 2010-09 Prenatal diagnosis of persistent cloaca with hydrometrocolpos and ascites by magnetic resonance imaging in one fetus of a dizygotic twin pregnancy 陳持平(Chih-Ping Chen)*; (Yu-Peng Liu); (Tung-Yao Chang); 蔡輔仁(Fuu-Jen Tsai); (Chen-Yu Chen); (Pei-Chen Wu); (Teresa Hsiao-Tien Chen); (Wayseen Wang)
國立臺灣大學 1992 Prenatal Diagnosis of Placental Chorioangioma: A Case Report 黃文章; 柯滄銘; SU, CHU'NG-GUEI; HWANG, WEN-JANG; CHANG, CHUNG-CHING; KO, TSANG-MING
國立成功大學 2014-04 Prenatal diagnosis of Prader-Willi syndrome and Angelman syndrome for fetuses with suspicious deletion of chromosomal region 15q11-q13 Chang, Chia-Wei; Hsu, Hui-Kuo; Kao, Chiu-Ching; Huang, Jyun-Yuan; Kuo, Pao-Lin

显示项目 683011-683060 / 2349128 (共46983页)
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每页显示[10|25|50]项目