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显示项目 682801-682850 / 2349128 (共46983页)
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机构	日期	题名	作者
臺北醫學大學	2014	Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 15	Chen, Chih-Ping;Chen, Ming;Su, Yi-Ning;Chern, Schu-Rern;Wu, Peih-Shan;Chang, Shun-Ping;Kuo, Yu-Ling;Chen, Wen-Lin;Wang, Wayseen
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)
臺大學術典藏	2018-09-10T15:02:34Z	Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 15	Chen, C.-P.;Chen, M.;Su, Y.-N.;Chern, S.-R.;Wu, P.-S.;Chang, S.-P.;Kuo, Y.-L.;Chen, W.-L.;Wang, W.; MING CHEN
亞洲大學	2017-08	Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 16	Wang, 陳持平；Chih-Ping Chen；Tsang-Ming K；Tsang-Ming Ko；Schu-Rern Ch；Schu-Rern Chern；Shin-Wen Che；Shin-Wen Chen；Shih-Ting La；Shih-Ting Lai；Peih-Shan Wu；Peih-Shan Wu；Chien-Wen Ya；Chien-Wen Yang；Chen-Wen Pan；Chen-Wen Pan；Wayseen Wang；Wayseen
亞洲大學	2017-04	Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 2	陳持平；Chih-Ping Chen；Ming Chen；Ming Chen；Shun-Ping Ch；Shun-Ping Chang；Fang-Yu Hung；Fang-Yu Hung；Meng-Ju Lee；Meng-Ju Lee；Schu-Rern Ch；Schu-Rern Chern；Peih-Shan Wu；Peih-Shan Wu；Yen-Ni Chen；Yen-Ni Chen；, ；Shin-Wen Chen,；,；Chen-Chi Lee,；Dai-Dyi Town；Dai-Dyi Town；Meng-Shan Le；Meng-Shan Lee；Wen-Lin Chen；Wen-Lin Chen；Wayseen Wang；Wayseen Wang
臺大學術典藏	2018-09-10T18:06:25Z	Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 2	Chen, C.-P. And Chen, M. And Chang, S.-P. And Hung, F.-Y. And Lee, M.-J. And Chern, S.-R. And Wu, P.-S. And Chen, Y.-N. And Chen, S.-W. And Lee, C.-C. And Town, D.-D. And Chen, W.-L. And Wang, W.; MING CHEN
臺大學術典藏	2018-09-10T18:06:25Z	Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 21	Chen, C.-P. And Chen, M. And Chern, S.-R. And Chang, S.-P. And Chen, S.-W. And Lai, S.-T. And Chen, W.-L. And Lee, M.-S. And Wang, W.; MING CHEN
亞洲大學	2017-08	Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 21q11.2-q21.1 and a literature review	Wang；, 陳持平；Chih-Ping Chen；Ming Chen；Ming Chen；Chia-Hsun Wu；Chia-Hsun Wu；Chen-Ju Lin；Chen-Ju Lin；Schu-Rern Ch；Schu-Rern Chern；Peih-Shan Wu；Peih-Shan Wu；Yen-Ni Chen；Yen-Ni Chen；Shin-Wen Che；Shin-Wen Chen；Shun-Ping Ch；Shun-Ping Chang；Li-Feng Chen；Li-Feng Chen；Wayseen Wang；Wayseen
臺大學術典藏	2018-09-10T18:06:25Z	Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 21q11.2-q21.1 and a literature review	Chen, C.-P. And Chen, M. And Wu, C.-H. And Lin, C.-J. And Chern, S.-R. And Wu, P.-S. And Chen, Y.-N. And Chen, S.-W. And Chang, S.-P. And Chen, L.-F. And Wang, W.; MING CHEN
亞洲大學	2013-09	Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 22 associated with cat eye syndrome	陳持平;Chen, Chih-Ping;Tsang-Ming, K;Ko, Tsang-Ming;Chen, Yi-Yung;Su, Jun-Wei;Wang, Wayseen;
亞洲大學	2019-11	Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 3	陳持平;Chen, Chih-Ping;Tsang-Ming, K;Ko, Tsang-Ming;Chen, Chen-Yu;Chen, Chen-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;Pan, Chen-Wen;Pan, Chen-Wen;Wang, Wayseen;Wang, Wayseen
亞洲大學	2012-09	Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 2	陳持平;Chen, Chih-Ping;Jun-Wei Su, ;Alan Hwa-Ruey Hsieh, ;Hsieh, Alex Hwa-Jiun;Wang, Wayseen
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)
亞洲大學	2011-06	Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 4	陳持平;Chen, Chih-Ping
國立臺灣大學	2011	Prenatal Diagnosis and Molecular Cytogenetic Characterization of Mosaicism for a Small Supernumerary Marker Chromosome Derived from Ring Chromosome 4	陳持平; 陳明; 蘇怡寧; 蔡輔仁; 陳樹人; 吳佩臻; 陳麗鳳; 王偉信; CHEN, CHIH-PING; CHEN, MING; SU, YI-NING; TSAI, FUU-JEN; CHERN, SCHU-RERN; WU, PEI-CHEN; CHEN, LI-FENG; WANG, WAYSEEN
臺大學術典藏	2018-09-10T08:50:12Z	Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 4	Chen, W.-L.;Pan, C.-W.;Chen, Chih-Ping;Chen, Ming;Su, Yi-Ning;Tsai, Fuu-Jen;Chern, Schu-Rern;Wu, Pei-Chen;Chen, Li-Feng;Wang, Wayseen; CHEN, CHIH-PING;CHEN, MING;SU, YI-NING;TSAI, FUU-JEN;CHERN, SCHU-RERN;WU, PEI-CHEN;CHEN, LI-FENG;WANG, WAYSEEN; 陳持平;陳明;蘇怡寧;蔡輔仁;陳樹人;吳佩臻;陳麗鳳;王偉信; MING CHEN; CHEN, CHIH-PING; CHEN, MING; SU, YI-NING; TSAI, FUU-JEN; CHERN, SCHU-RERN; WU, PEI-CHEN; CHEN, LI-FENG; WANG, WAYSEEN
亞洲大學	2020-01-20	Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for r(13), monosomy 13 and idic r(13) by amniocentesis	Ch, Chih-Ping;Chen, Chih-Ping;Chen, Chen-Yu;Chen, Chen-Yu;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Che, Shin-Wen;Chen, Shin-Wen;Lee, Chen-Chi;Lee, Chen-Chi;Chen, Li-Feng;Chen, Li-Feng;Wang, Wayseen;Wang, Wayseen
亞洲大學	2016-10	Prenatal diagnosis and molecular cytogenetic characterization of rec(10)dup(10p)inv(10)(p11.2q26.3) in a fetus associated with paternal pericentirc inversion	陳持平;Chen, Chih-Ping;*;Tsang-Ming, K;Ko, Tsang-Ming;Su, Yi-Ning;Su, Yi-Ning;Wa, Liang-Kai;Wang, Liang-Kai;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Chen, Yen-Ni;Chen, Yen-Ni;Che, Shin-Wen;Che, Shin-Wen;Town, Dai-Dyi;Town, Dai-Dyi;Chen, Li-Feng;Chen, Li-Feng;Ya, Chien-Wen;Yang, Chien-Wen;Wang, Wayseen;Wang, Wayseen
亞洲大學	2012-06	Prenatal diagnosis and molecular genetic analysis of short rib-polydactyly syndrome type III (Verma-Naumoff) in a second-trimester fetus with a homozygous splice site mutation in intron 4 in the NEK1 gene	陳持平;Chen, Chih-Ping
中國醫藥大學	2012-06	Prenatal diagnosis and molecular genetic analysis of short rib-polydactyly syndrome type III (Verma-Naumoff) in a second-trimester fetus with a homozygous splice site mutation in intron 4 in the NEK1 gene	陳持平(Chih-Ping Chen)*;(Schu-Rern Chern);(Tung-Yao Chang);(Yi-Ning Su);(Yi-Yung Chen);(Jun-Wei Su);(Wayseen Wang)
臺大學術典藏	2018-09-10T06:48:26Z	Prenatal diagnosis and perinatal outcome of facial clefts	Pan, Y.-J. and Shih, J.-C. and Lee, C.-N. and Shyu, M.-K. and Hwa, H.-L. and Chen, H.-Y. and Hsieh F.-, J.; HSIAO-LIN HWA
臺大學術典藏	2018-09-10T06:50:05Z	Prenatal diagnosis and perinatal outcome of facial clefts	Pan, Y.-J. and Shih, J.-C. and Lee, C.-N. and Shyu, M.-K. and Hwa, H.-L. and Chen, H.-Y. and Hsieh F.-, J.; MING-KWANG SHYU
臺大學術典藏	2018-09-10T07:14:01Z	Prenatal diagnosis and perinatal outcome of facial clefts	Pan, Y.-J. and Shih, J.-C. and Lee, C.-N. and Shyu, M.-K. and Hwa, H.-L. and Chen, H.-Y. and Hsieh F.-, J.; CHIEN-NAN LEE
臺大學術典藏	2020-02-03T08:15:26Z	Prenatal diagnosis and perinatal outcome of facial clefts	Pan Y.-J.; Shih J.-C.; Lee C.-N.; Shyu M.-K.; HSIAO-LIN HWA; Chen H.-Y.; Hsieh F.- J.
臺大學術典藏	2020-02-12T04:06:51Z	Prenatal diagnosis and perinatal outcome of facial clefts	Hsieh F.- J.;Chen H.-Y;Hwa H.-L;Shyu M.-K;CHIEN-NAN LEE;Shih J.-C;Pan Y.-J; Pan Y.-J; Shih J.-C; CHIEN-NAN LEE; Shyu M.-K; Hwa H.-L; Chen H.-Y; Hsieh F.- J.
臺大學術典藏	2020-02-14T05:49:52Z	Prenatal diagnosis and perinatal outcome of facial clefts	Pan Y.-J; Shih J.-C; Lee C.-N; MING-KWANG SHYU; Hwa H.-L; Chen H.-Y; Hsieh F.- J.
國立臺灣大學	1987	Prenatal Diagnosis and Postnatal Management of Surgically Correctable Fatal Malformations	Hsieh, F. J.; Lin, C. R.; 陳維昭; 陳秋江; Tsai, T. C.; Hsieh, F. J.; Lin, C. R.; Chen, Wei-Jao; Chen, Chiu-Chiang; Tsai, T. C.
國立臺灣大學	1989	Prenatal Diagnosis and Postnatal Management of Surgically Correctable Fetal Malformations	謝豐舟; 林啟瑞; 陳維昭; 陳秋江; 蔡崇璋; HSIEH, FON-JOU; LIN, CHII-RUAY; CHEN, WEI-JAO; CHEN, CHIU-CHIANG; TSAI, TSONG-CHANG
臺大學術典藏	2018-09-10T04:05:34Z	Prenatal diagnosis and treatment of fetal long QT syndrome: A case report	Chang, I.-K. and Shyu, M.-K. and Lee, C.-N. and Kau, M.-L. and Ko, Y.-H. and Chow, S.-N. and Hsieh, F.-J.; MING-KWANG SHYU; CHIEN-NAN LEE
國立臺灣大學	2002	Prenatal Diagnosis and Treatment of Fetal Long Qt Syndrome: A Case Report	張銀光; 徐明洸; 李建南; 高妙玲; 柯玉雪; 周松男; 謝豐舟; CHANG, ING-KUANG; SHYU, MING-KWANG; LEE, CHIEN-NAN; KAO, MIAO-LING; KO, YU-HSUEH; CHOW, SONG-NAN; HSIEH, FON-JOU
臺大學術典藏	2020-02-12T04:06:39Z	Prenatal diagnosis and treatment of fetal long QT syndrome: A case report	Hsieh F.-J.;Chow S.-N;Ko Y.-H;Kau M.-L;CHIEN-NAN LEE;Shyu M.-K;Chang I.-K; Chang I.-K; Shyu M.-K; CHIEN-NAN LEE; Kau M.-L; Hsieh F.-J.; Ko Y.-H; Chow S.-N
臺大學術典藏	2020-02-14T05:49:48Z	Prenatal diagnosis and treatment of fetal long QT syndrome: A case report	MING-KWANG SHYU; Lee C.-N; Kau M.-L; Ko Y.-H; Chow S.-N; Hsieh F.-J.; Chang I.-K;Ming-Kwang Shyu;Lee C.-N;Kau M.-L;Ko Y.-H;Chow S.-N;Hsieh F.-J.; Chang I.-K
臺大學術典藏	2021-02-04T06:05:22Z	Prenatal diagnosis and treatment of fetal long QT syndrome: A case report	Chang I.-K.;Shyu M.-K.;Chien-Nan Lee;Kau M.-L.;Ko Y.-H.;Chow S.-N.;Hsieh F.-J.; Chang I.-K.; Shyu M.-K.; CHIEN-NAN LEE; Kau M.-L.; Ko Y.-H.; Chow S.-N.; Hsieh F.-J.
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	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	2022-03-10T07:58:57Z	Prenatal diagnosis by transabdominal chorionic villus sampling in the second and third trimesters	Ko T.-M.; LI-HUI TSENG; Hwa H.-L.; Lee T.-Y.; Chuang S.-M.
亞洲大學	2016-02	Prenatal diagnosis of 22q11.2 deletion syndrome associated with right aortic arch, left ductus arteriosus, cardiomegaly, and pericardial effusion	Chen), Yen-Ni Chen(Yen-Ni;陳持平*;Ko), Tsang-Ming K(Tsang-Ming;Wang), Liang-Kai Wa(Liang-Kai;Wu), Pei-Chen Wu(Pei-Chen;Chang), Tung-Yao Cha(Tung-Yao;Wu), Peih-Shan Wu(Peih-Shan;Yang), Chien-Wen Ya(Chien-Wen;Wang), Wayseen Wang(Wayseen
亞洲大學	2016-02	Prenatal diagnosis of 22q11.2 deletion syndrome associated with right aortic arch, left ductus arteriosus, cardiomegaly, and pericardial effusion	Chen, Yen-Ni;Chen, Yen-Ni;陳持平*;Tsang-Ming, K;Ko, Tsang-Ming;Wa, Liang-Kai;Wang, Liang-Kai;Wu, Pei-Chen;Wu, Pei-Chen;Cha, Tung-Yao;Chang, Tung-Yao;Wu, Peih-Shan;Wu, Peih-Shan;Ya, Chien-Wen;Yang, Chien-Wen;Wang, Wayseen;Wang, Wayseen
亞洲大學	2016-02	Prenatal diagnosis of 22q11.2 deletion syndrome associated with right aortic arch, left ductus arteriosus, cardiomegaly, and pericardial effusion	Wang；, Yen-Ni Chen；Yen-Ni Chen；陳持平*；Tsang-Ming K；Tsang-Ming Ko；Liang-Kai Wa；Liang-Kai Wang；Pei-Chen Wu；Pei-Chen Wu；Tung-Yao Cha；Tung-Yao Chang；Peih-Shan Wu；Peih-Shan Wu；Chien-Wen Ya；Chien-Wen Yang；Wayseen Wang；Wayseen
臺大學術典藏	2020-02-14T02:50:41Z	Prenatal diagnosis of 46, XX/47, XXY mosaicism: A case report	Cheng W.?F.; Huang S.?C.; Ko T.?M.
亞洲大學	2009-03	PRENATAL DIAGNOSIS OF 46,XX,DER(13;21)(Q10;Q10),+21 AND TRANSIENT ABNORMAL MYELOPOIESIS IN A FETUS WITH HEPATOSPLENOMEGALY AND SPONTANEOUS RESOLUTION OF FETAL ASCITES	Chen, CP (Chen, Chih-Ping); Tsai, FJ (Tsai, Fuu-Jen); Chern, SR (Chern, Schu-Rern); Chang, TY (Chang, Tung-Yao); Hsu, CY (Hsu, Chin-Yuan); Lin, HH (Lin, Hung-Hung); Wang, W (Wang, Wayseen)
亞洲大學	2009-03	PRENATAL DIAGNOSIS OF 46,XX,DER(13;21)(Q10;Q10),+21 AND TRANSIENT ABNORMAL MYELOPOIESIS IN A FETUS WITH HEPATOSPLENOMEGALY AND SPONTANEOUS RESOLUTION OF FETAL ASCITES	陳持平;Chen, Chih-Ping;Tsai, Fuu-Jen;Chern, Schu-Rern;Chang, Tung-Yao;Hsu, Chin-Yuan;Lin, Hung-Hung;Wang, Wayseen
中國醫藥大學	2009-03	Prenatal diagnosis of 46,XX,der(13;21)(q10;q10),+21 and transient abnormal myelopoiesis in a fetus with hepatosplenomegaly and spontaneous resolution of fetal ascites	陳持平(Chih-Ping Chen); 蔡輔仁(Fuu-Jen Tsai); (Schu-Rern Chern); (Tung-Yao Chang); (Chin-Yuan Hsu); (Hung-Hung Lin); (Wayseen Wang)
亞洲大學	2018-02	Prenatal diagnosis of a 0.7-Mb 17p13.3 microdeletion encompassing YWHAE and CRK but not PAFAH1B1 in a fetus without ultrasound abnormalities	陳持平;Chen, Chih-Ping;*;Tsang-Ming, K;Ko, Tsang-Ming;Wa, Liang-Kai;Wang, Liang-Kai;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Che, Shin-Wen;Chen, Shin-Wen;La, Shih-Ting;Lai, Shih-Ting;Chua, Tzu-Yun;Chuang, Tzu-Yun;Ya, Chien-Wen;Yang, Chien-Wen;Lee, Chen-Chi;Lee, Chen-Chi;Wang, Wayseen;Wang, Wayseen
亞洲大學	2017-12	Prenatal diagnosis of a 1.6-Mb 4p16.3 interstitial microdeletion encompassing FGFRL1 and TACC3 associated with bilateral cleft lip and palate of Wolf-Hirschhorn syndrome facial dysmorphism and short long bones	陳持平;Chen, Chih-Ping;Chen, Chen-Yu;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Che, Shin-Wen;Chen, Shin-Wen;La, Shih-Ting;Lai, Shih-Ting;Chua, Tzu-Yun;Chuang, Tzu-Yun;Ya, Chien-Wen;Yang, Chien-Wen;Chen, Li-Feng;Wang, Wayseen
亞洲大學	2009-12	Prenatal diagnosis of a 22q11.2 microdeletion in a fetus with double-outlet right ventricle, pulmonary stenosis and a ventricular septal defect by array comparative genomic hybridization	陳持平;Chen, Chih-Ping;Su, Yi-Ning;Chang, Tung-Yao;Chern, Schu-Rern;Tsai, Fuu-Jen;Hwang, Jonathan Kwei;Wang, Wayseen
亞洲大學	2018-08	Prenatal diagnosis of a 3.2-Mb 2p16.1-p15 duplication associated with familial intellectual disability	陳持平;Chen, Chih-Ping;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Che, Shin-Wen;Chen, Shin-Wen;La, Shih-Ting;Lai, Shih-Ting;Chua, Tzu-Yun;Chuang, Tzu-Yun;Chen, Wen-Lin;Chen, Wen-Lin;Ya, Chien-Wen;Yang, Chien-Wen;Wang, Wayseen;Wang, Wayseen
國立臺灣大學	2010	Prenatal Diagnosis of a 4.9-Mb Deletion of 10q11.21 -> Q11.23 by Array Comparative Genomic Hybridization	陳持平; 蘇怡寧; 陳樹人; 蔡輔仁; 徐金源; 李貞姫; 王偉信; CHEN, CHIH-PING; SU, YI-NING; CHERN, SCHU-RERN; TSAI, FUU-JEN; HSU, CHIN-YUAN; LEE, CHEN-CHI; WANG, WAYSEEN
中國醫藥大學	2010-03	Prenatal diagnosis of a 4.9-Mb deletion of 10q11.21->q11.23 by array comparative genomic hybridization	陳持平(Chih-Ping Chen)*; (Yi-Ning Su); (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Chin-Yuan Hsu); (Chen-Chi Lee); (Wayseen Wang)

显示项目 682801-682850 / 2349128 (共46983页)
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