| 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 |
| 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. |
| 亞洲大學 |
2010-09 |
Prenatal diagnosis of rhabdomyomas and cerebral tuberous sclerosis by magnetic resonance imaging in one fetus of a dizygotic twin pregnancy associated with a frameshift mutation in the TSC2 gene
|
陳持平;Chen, Chih-Ping;Su, Yi-Ning;Chang, Tung-Yao;Liu, Yu-Peng;Tsai, Fuu-Jen;Chen, Ming-Ren;Hwang, Jonathan Kwei;Chen, Teresa Hsiao-Tien;Wang, Wayseen |
| 國立臺灣大學 |
2010 |
Prenatal Diagnosis of Rhabdomyomas and Cerebral Tuberous Sclerosis by Magnetic Resonance Imaging in One Fetus of a Dizygotic Twin Pregnancy Associated with a Frameshift Mutation in the Tsc2 Gene
|
陳持平; 蘇怡寧; 張東曜; 劉育朋; 蔡輔仁; 陳銘仁; 王偉信; CHEN, CHIH-PING; SU, YI-NING; CHANG, TUNG-YAO; LIU, YU-PENG; TSAI, FUU-JEN; CHEN, MING-REN; WANG, WAYSEEN |
| 中國醫藥大學 |
2010-09 |
Prenatal diagnosis of rhabdomyomas and cerebral tuberous sclerosis by magnetic resonance imaging in one fetus of a dizygotic twin pregnancy associated with a frameshift mutation in the TSC2 gene
|
陳持平(Chih-Ping Chen)*; (Yi-Ning Su); (Tung-Yao Chang); (Yu-Peng Liu); 蔡輔仁(Fuu-Jen Tsai); (Ming-Ren Chen); (Jonathan Kwei Hwang); (Teresa Hsiao-Tien Chen); (Wayseen Wang) |
| 國立臺灣大學 |
2003 |
Prenatal Diagnosis of Right Pulmonary Agenesis Associated with Vacterl Sequence
|
施景中; SHIH, JIN-CHUNG |
| 臺大學術典藏 |
2021-02-04T06:46:56Z |
Prenatal diagnosis of right pulmonary agenesis associated with VACTERL sequence [3]
|
Chen C.-P.;Jin-Chung Shih;Chang J.-H.;Lin Y.-H.;Wang W.; Chen C.-P.; JIN-CHUNG SHIH; Chang J.-H.; Lin Y.-H.; Wang W. |
| 亞洲大學 |
2013-04 |
Prenatal diagnosis of ring chromosome 2 with lissencephaly and 2p25.3 and 2q37.3 microdeletions detected using array comparative genomic hybridization
|
陳持平;Chen, Chih-Ping;Lin, Chen-Ju;Lin, Chen-Ju;Cha, Tung-Yao;Chang, Tung-Yao;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Chen, Yu-Ting;Chen, Yu-Ting;Su, Jun-Wei;Su, Jun-Wei;Lee, Chen-Chi;Lee, Chen-Chi;Chen, Li-Feng;Chen, Li-Feng;Wang, Wayseen;Wang, Wayseen |
| 中國醫藥大學 |
2013-04 |
Prenatal diagnosis of ring chromosome 2 with lissencephaly and 2p25.3 and 2q37.3 microdeletions detected using array comparative genomic hybridization
|
陳持平(Chih-Ping Chen)*;(Chen-Ju Lin);(Tung-Yao Chang);(Schu-Rern Chern);(Peih-Shan Wu);(Yu-Ting Chen);(Jun-Wei Su);(Chen-Chi Lee);(Li-Feng Chen);(Wayseen Wang) |
| 亞洲大學 |
2010-09 |
Prenatal diagnosis of satellited 21q derived from pericentric inversion involving the satellite stalk region and terminal 21q
|
陳持平;Chen, Chih-Ping;Tsai, Fuu-Jen;Lee, Chen-Chi;Chen, Wen-Lin;Pan, Chen-Wen;Wu, Pei-Chen;Wang, Wayseen |
| 中國醫藥大學 |
2010-09 |
Prenatal diagnosis of satellited 21q derived from pericentric inversion involving the satellite stalk region and terminal 21q
|
陳持平(Chih-Ping Chen)*; 蔡輔仁(Fuu-Jen Tsai); (Chen-Chi Lee); (Wen-Lin Chen); (Chen-Wen Pan); (Pei-Chen Wu); (Wayseen Wang) |
| 國立中山大學 |
2004 |
Prenatal diagnosis of sharp-angled lumbosacral kyphosis with myelomeningocele and spina bifida in a fetus
|
F.N. Cho;Y.Y. Kan;T.L. Yang;H.P. Huang;P.H. Hsu;M.H. Tai |
