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Showing items 682776-682825 of 2349128 (46983 Page(s) Totally)
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| 中國醫藥大學 |
2014-06 |
Prenatal diagnosis and molecular cytogenetic characterization of chromosome 22q11.2 deletion syndrome associated with congenital heart defects
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Yu-Ling Kuo;陳持平(Chih-Ping Chen)*;(Liang-Kai Wang);(Tsang-Ming Ko);(Tung-Yao Chang);(Schu-Rern Chern);(Peih-Shan Wu);(Yu-Ting Chen);(Shu-Yuan Chang) |
| 亞洲大學 |
2017-04 |
Prenatal diagnosis and molecular cytogenetic characterization of concomitant familial small supernumerary marker chromosome derived from chromosome 4q ；4q11.1-q13.2 and 5q13.2 microdeletion with no apparent phenotypic abnormality
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Lee；；；；, 陳持平；Chih-Ping Chen；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；Chen-Chi Lee；Chen-Chi Lee；Meng-Shan Le；Meng-Shan |
| 亞洲大學 |
2020-01-20 |
Prenatal diagnosis and molecular cytogenetic characterization of de novo distal 5p deletion and distal 22q duplication
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Ch, Chih-Ping;Chen, Chih-Ping;Hua, Jian-Pei;Huang, Jian-Pei;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Che, Shin-Wen;Chen, Shin-Wen;Wu, Fang-Tzu;Wu, Fang-Tzu;Chen, Wen-Lin;Chen, Wen-Lin;Le, Meng-Shan;Lee, Meng-Shan;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2016-04 |
Prenatal diagnosis and molecular cytogenetic characterization of de novo partial monosomy 3p (3p26.3->pter) and partial trisomy 16q (16q23.1->qter)
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Chen)*, 陳持平(Chih-Ping;Hung), Fang-Yu Hung(Fang-Yu;Chern), Schu-Rern Ch(Schu-Rern;Wu), Peih-Shan Wu(Peih-Shan;Chen), Yen-Ni Chen(Yen-Ni;Chen), Shin-Wen Che(Shin-Wen;Lee), Chen-Chi Lee(Chen-Chi;Wang), Wayseen Wang(Wayseen |
| 亞洲大學 |
2016-04 |
Prenatal diagnosis and molecular cytogenetic characterization of de novo partial monosomy 3p (3p26.3->pter) and partial trisomy 16q (16q23.1->qter)
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陳持平;Chen, Chih-Ping;*;Hung, Fang-Yu;Hung, Fang-Yu;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Chen, Yen-Ni;Chen, Yen-Ni;Che, Shin-Wen;Chen, Shin-Wen;Lee, Chen-Chi;Lee, Chen-Chi;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2016-04 |
Prenatal diagnosis and molecular cytogenetic characterization of de novo partial monosomy 3p (3p26.3->pter) and partial trisomy 16q (16q23.1->qter)
|
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；Chen-Chi Lee；Chen-Chi Lee；Wayseen Wang；Wayseen |
| 亞洲大學 |
2016-04 |
Prenatal diagnosis and molecular cytogenetic characterization of de novo partial monosomy 3p ;3p26.3->pter; and partial trisomy 16q ;16q23.1->qter;
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陳持平;Chen, Chih-Ping;*;Hung, Fang-Yu;Hung, Fang-Yu;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Chen, Yen-Ni;Chen, Yen-Ni;Che, Shin-Wen;Chen, Shin-Wen;Lee, Chen-Chi;Lee, Chen-Chi;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2013-03 |
Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 12q (12q24.21->qter) and partial monosomy 6q (6q27->qter) associated with coarctation of the aorta, ventriculomegaly and thickened nuchal fold
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陳持平;Chen, Chih-Ping;Yi-Yung Chen;Schu-Rern Chern;Peih-Shan Wu;Jun-Wei Su;Yu-Ting Chen;Li-Feng Chen;Wayseen Wang |
| 中國醫藥大學 |
2013-03 |
Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 12q (12q24.21->qter) and partial monosomy 6q (6q27->qter) associated with coarctation of the aorta, ventriculomegaly and thickened nuchal fold
|
陳持平(Chih-Ping Chen)*;(Yi-Yung Chen);(Schu-Rern Chern);(Peih-Shan Wu);(Jun-Wei Su);(Yu-Ting Chen);(Li-Feng Chen);(Wayseen Wang) |
| 國立臺灣大學 |
2010 |
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
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陳持平; 陳明; 蘇怡寧; 蔡輔仁; 陳樹人; 徐金源; 吳佩臻; 李東杰; 馬國欽; 王偉信; CHEN, CHIH-PING; CHEN, MING; SU, YI-NING; TSAI, FUU-JEN; CHERN, SCHU-RERN; HSU, CHIN-YUAN; WU, PEI-CHEN; LEE, DONG-JAY; MA, GWO-CHIN; WANG, WAYSEEN |
| 亞洲大學 |
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
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陳持平;Chen, Chih-Ping;Chen, Ming;Su, Yi-Ning;Tsai, Fuu-Jen;Chern, Schu-Rern;Hsu, Chin-Yuan;Wu, Pei-Chen;Town, Dai-Dyi;Lee, Dong-Jay;Ma, Gwo-Chin;Wang, Wayseen |
| 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 |
2014-02 |
Prenatal diagnosis and molecular cytogenetic characterization of de novo pure partial trisomy 6p associated with microcephaly, craniosynostosis and abnormal maternal serum biochemistry
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陳持平;Chen, Chih-Ping;Ming Cheng;Chen-Yu Chen;Schu-Rern Chern;Peih-Shan Wu;Shun-Ping Chang;Yu-Ling Kuo;Wen-Lin Chen;Chen-Wen Pan;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
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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 |
2018-09-10T15:02:34Z |
Prenatal diagnosis and molecular cytogenetic characterization of de novo pure partial trisomy 6p associated with microcephaly, craniosynostosis and abnormal maternal serum biochemistry
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Chen, C.-P.;Chen, M.;Chen, C.-Y.;Chern, S.-R.;Wu, P.-S.;Chang, S.-P.;Kuo, Y.-L.;Chen, W.-L.;Pan, C.-W.;Wang, W.; MING CHEN |
| 亞洲大學 |
2017-04 |
Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaic trisomy 12 at amniocentesis associated with a favorable pregnancy outcome
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Wang, 陳持平；Chih-Ping Chen；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；Chen-Wen Pan；Chen-Wen Pan；Chien-Wen Ya；Chien-Wen Yang；Wayseen Wang；Wayseen |
| 亞洲大學 |
2017-12 |
Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaicism for tetrasomy 18p at amniocentesis in a pregnancy with a favorable outcome
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陳持平;Chen, Chih-Ping;Tsang-Ming, K;Ko, Tsang-Ming;Chen, Yi-Yung;Ch, Schu-Rern;Chern, Schu-Rern;Che, Shin-Wen;Chen, Shin-Wen;La, Shih-Ting;Lai, Shih-Ting;Chua, Tzu-Yun;Chuang, Tzu-Yun;Ya, Chien-Wen;Yang, Chien-Wen;Pan, Chen-Wen;Wang, Wayseen |
| 亞洲大學 |
2016-04 |
Prenatal diagnosis and molecular cytogenetic characterization of low-level true mosaicism for trisomy 21 using uncultured amniocytes
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Chen)*, 陳持平(Chih-Ping;Wang), Yeou-Lih Wan(Yeou-Lih;Chern), Schu-Rern Ch(Schu-Rern;Wu), Peih-Shan Wu(Peih-Shan;Chen), Yen-Ni Chen(Yen-Ni;Chen), Shin-Wen Che(Shin-Wen;Chen), Li-Feng Chen(Li-Feng;Lee), Meng-Shan Le(Meng-Shan;Yang), Chien-Wen Ya(Chien-Wen;Wang), Wayseen Wang(Wayseen |
| 亞洲大學 |
2016-04 |
Prenatal diagnosis and molecular cytogenetic characterization of low-level true mosaicism for trisomy 21 using uncultured amniocytes
|
陳持平;Chen, Chih-Ping;*;Wan, Yeou-Lih;Wang, Yeou-Lih;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Chen, Yen-Ni;Chen, Yen-Ni;Che, Shin-Wen;Chen, Shin-Wen;Chen, Li-Feng;Chen, Li-Feng;Le, Meng-Shan;Lee, Meng-Shan;Ya, Chien-Wen;Yang, Chien-Wen;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2016-04 |
Prenatal diagnosis and molecular cytogenetic characterization of low-level true mosaicism for trisomy 21 using uncultured amniocytes
|
Wang；, 陳持平；Chih-Ping Chen；*；Yeou-Lih Wan；Yeou-Lih Wang；Schu-Rern Ch；Schu-Rern Chern；Peih-Shan Wu；Peih-Shan Wu；Yen-Ni Chen；Yen-Ni Chen；Shin-Wen Che；Shin-Wen Chen；Li-Feng Chen；Li-Feng Chen；Meng-Shan Le；Meng-Shan Lee；Chien-Wen Ya；Chien-Wen Yang；Wayseen Wang；Wayseen |
| 亞洲大學 |
2013-10 |
Prenatal diagnosis and molecular cytogenetic characterization of mosaic ring chromosome 13
|
陳持平;Chen, Chih-Ping;Chin-Han Tsai;Schu-Rern Chern;Peih-Shan Wu;Jun-Wei Su;Chen-Chi Lee;Yu-Ting Chen;Wen-Lin Chen;Li-Feng Chen;Wayseen Wang |
| 亞洲大學 |
2013-10 |
Prenatal diagnosis and molecular cytogenetic characterization of mosaic ring chromosome 13
|
陳持平;Chen, Chih-Ping;Chin-Han Tsai;Schu-Rern Chern;Peih-Shan Wu;Jun-Wei Su;Chen-Chi Lee;Yu-Ting Chen;Wen-Lin Chen;Li-Feng Chen;Wayseen Wang |
| 亞洲大學 |
2017-06 |
Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 11
|
Wang, 陳持平；Chih-Ping Chen；Ming Chen；Ming Chen；Pu-Tsui Wang；Pu-Tsui Wang；Schu-Rern Ch；Schu-Rern Chern；Shin-Wen Che；Shin-Wen Chen；Shih-Ting La；Shih-Ting Lai；Peih-Shan Wu；Peih-Shan Wu；Shun-Ping Ch；Shun-Ping Chang；Chen-Wen Pan；Chen-Wen Pan；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 11
|
Chen, C.-P. And Chen, M. And Wang, P.-T. And Chern, S.-R. And Chen, S.-W. And Lai, S.-T. And Wu, P.-S. And Chang, S.-P. And Pan, C.-W. And Wang, W.; MING CHEN |
| 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
|
陳持平;Chen, Chih-Ping;Chen, Ming;Chen, Ming;Su, Yi-Ning;Chern, Schu-Rern;Wu, Peih-Shan;Ch, 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 |
2020-02-14T05:49:52Z |
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. |
Showing items 682776-682825 of 2349128 (46983 Page(s) Totally)
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