| 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 |
| 國立臺灣大學 |
2008 |
Prenatal Diagnosis of Progressive Familial Intrahepatic Cholestasis Type 2
|
陳思達; 陳慧玲; 蘇怡寧; 劉有容; 倪衍玄; 許宏遠; 朱家祥; 王乃雩; 張美惠; CHEN, SZU-TAH; CHEN, HUEY-LING; SU, YI-NING; LIU, YU-JUNG; NI, YEN-HSUAN; HSU, HONG-YUAN; CHU, CHIA-HSIANG; WANG, NAI-YU; CHANG, MEI-HWEI |
| 臺大學術典藏 |
2018-09-10T07:12:55Z |
Prenatal diagnosis of progressive familial intrahepatic cholestasis type 2
|
Chen, S.-T. and Chen, H.-L. and Su, Y.-N. and Liu, Y.-J. and Ni, Y.-H. and Hsu, H.-Y. and Chu, C.-S. and Wang, N.-Y. and Chang, M.-H.; HONG-YUAN HSU; MEI-HWEI CHANG; Yen-Hsuan Ni |
| 臺大學術典藏 |
2019-12-25T04:04:23Z |
Prenatal diagnosis of progressive familial intrahepatic cholestasis type 2
|
Chen S.-T.;Chen H.-L.;Su Y.-N.;Liu Y.-J.;Ni Y.-H.;Hong-Yuan Hsu;Chu C.-S.;Wang N.-Y.;Chang M.-H.; Chen S.-T.; Chen H.-L.; Su Y.-N.; Liu Y.-J.; Ni Y.-H.; HONG-YUAN HSU; Chu C.-S.; Wang N.-Y.; Chang M.-H. |
| 臺大學術典藏 |
2020-03-10T03:30:32Z |
Prenatal diagnosis of progressive familial intrahepatic cholestasis type 2
|
Su Y.-N.; HUEY-LING CHEN; Chen S.-T.; Liu Y.-J.; Ni Y.-H.; Hsu H.-Y.; Chu C.-S.; Wang N.-Y.; Chang M.-H. |
| 臺大學術典藏 |
2021-01-04T07:36:08Z |
Prenatal diagnosis of progressive familial intrahepatic cholestasis type 2
|
Chen S.-T.;Chen H.-L.;Su Y.-N.;Liu Y.-J.;Ni Y.-H.;Hsu H.-Y.;Chu C.-S.;Wang N.-Y.;Mei-Hwei Chang; Chen S.-T.; Chen H.-L.; Su Y.-N.; Liu Y.-J.; Ni Y.-H.; Hsu H.-Y.; Chu C.-S.; Wang N.-Y.; MEI-HWEI CHANG |
| 臺大學術典藏 |
2020-12-28T08:14:42Z |
Prenatal diagnosis of progressive familial intrahepatic cholestasis type 2
|
Hsu H.-Y.; Chu C.-S.; Wang N.-Y.; Chang M.-H.; Chen S.-T.;Chen H.-L.;Su Y.-N.;Liu Y.-J.;Yen-Hsuan Ni;Hsu H.-Y.;Chu C.-S.;Wang N.-Y.;Chang M.-H.; Chen S.-T.; Chen H.-L.; Su Y.-N.; Liu Y.-J.; YEN-HSUAN NI |
| 臺大學術典藏 |
2020-02-12T04:05:51Z |
Prenatal diagnosis of proximal femoral focal deficiency: A case report andliterature review
|
Su Y.-N.;CHIEN-NAN LEE;Lin C.-H;Shih J.-C;Chung C.-H;Lin T.-H; Lin T.-H; Chung C.-H; Shih J.-C; Lin C.-H; CHIEN-NAN LEE; Su Y.-N. |
| 國立成功大學 |
2004-11 |
Prenatal diagnosis of radial agenesis in trisomy 18 using three-dimensional ultrasound
|
Huang, Yu-Fang; Chang, Chiung-Hsin; Yu, Chen-Hsiang; Chang, Fong-Ming |
| 亞洲大學 |
2013-03 |
Prenatal diagnosis of recurrent autosomal dominant osteogenesis imperfecta associated with unaffected parents and paternal gonadal mosaicism
|
陳持平;Chen, Chih-Ping;Li, Shuan-Pei;Lin, Shuan-Pei;Su, Yi-Ning;Su, Yi-Ning;Ch, Schu-Rern;Chern, Schu-Rern;Su, Jun-Wei;Su, Jun-Wei;Wang, Wayseen;Wang, Wayseen |
| 中國醫藥大學 |
2013-03 |
Prenatal diagnosis of recurrent autosomal dominant osteogenesis imperfecta associated with unaffected parents and paternal gonadal mosaicism
|
陳持平(Chih-Ping Chen)*;(Shuan-Pei Lin);(Yi-Ning Su);(Schu-Rern Chern);(Jun-Wei Su);(Wayseen Wang) |
| 臺大學術典藏 |
2018-09-10T05:46:35Z |
Prenatal diagnosis of recurrent idiopathic microcephaly: Report of a case
|
Chiang, L.-H. and Chang, M.-J. and Shyu, M.-K. and Lee, C.-N. and Shi, J.-C. and Lin, J.-H. and Lin, G.-J. and Hsieh, F.-J.; MING-KWANG SHYU |
| 臺大學術典藏 |
2018-09-10T06:07:10Z |
Prenatal diagnosis of recurrent idiopathic microcephaly: Report of a case
|
Chiang, L.-H. and Chang, M.-J. and Shyu, M.-K. and Lee, C.-N. and Shi, J.-C. and Lin, J.-H. and Lin, G.-J. and Hsieh, F.-J.; CHIEN-NAN LEE |
| 臺大學術典藏 |
2020-02-12T04:06:57Z |
Prenatal diagnosis of recurrent idiopathic microcephaly: Report of a case
|
Hsieh F.-J.;Lin G.-J;Lin J.-H;Shi J.-C;CHIEN-NAN LEE;Shyu M.-K;Chang M.-J;Chiang L.-H; Chiang L.-H; Chang M.-J; Shyu M.-K; CHIEN-NAN LEE; Shi J.-C; Lin J.-H; Lin G.-J; Hsieh F.-J. |
| 臺大學術典藏 |
2020-02-14T05:49:53Z |
Prenatal diagnosis of recurrent idiopathic microcephaly: Report of a case
|
Chiang L.-H;Chang M.-J;Ming-Kwang Shyu;Lee C.-N;Shi J.-C;Lin J.-H;Lin G.-J;Hsieh F.-J.; Chiang L.-H; Chang M.-J; MING-KWANG SHYU; Lee C.-N; Shi J.-C; Lin J.-H; Lin G.-J; Hsieh F.-J. |
| 臺大學術典藏 |
2021-02-04T06:05:31Z |
Prenatal diagnosis of recurrent idiopathic microcephaly: Report of a case
|
Chiang L.-H.;Chang M.-J.;Shyu M.-K.;Chien-Nan Lee;Shi J.-C.;Lin J.-H.;Lin G.-J.;Hsieh F.-J.; Chiang L.-H.; Chang M.-J.; Shyu M.-K.; CHIEN-NAN LEE; Shi J.-C.; Lin J.-H.; Lin G.-J.; Hsieh F.-J. |
