| 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 |
