公開日期 | 標題 | 作者 | 來源出版物 | scopus | WOS | 全文 |
2022 | A polymer donor with versatility for fabricating high-performance ternary organic photovoltaics | Jiang B.-H; Peng Y.-J; Su Y.-W; Chang J.-F; Chueh C.-C ; Shieh T.-S; Huang C.-I ; Chen, Chih-Ping | Chemical Engineering Journal | 23 | 21 | |
2007 | Prenatal Diagnosis and Genetic Counseling of Mucopolysaccharidosis Type Ii (Hunter Syndrome) | CHEN, CHIH-PING; LIN, SHUAN-PEI; TZEN, CHIN-YUAN; HWU, WUH-LIANG; CHERN, SCHU-RERN; WANG, WAY-SEEN | GENETIC COUNSELING | | | |
2005 | Prenatal diagnosis and molecular cytogenetic analysis of partial monosomy 10q (10q25.3-->qter) and partial trisomy 18q (18q23-->qter) in a fetus associated with cystic hygroma and ambiguous genitalia | Chen, Chih-Ping; Chern, Schu-Rern; Wang, Tzu-Hao; Hsueh, Ding-Wei; Lee, Chen-Chi; Town, Dai-Dyi; Wang, Wayseen; TSANG-MING KO | Prenatal diagnosis | 19 | 18 | |
2020 | Prenatal diagnosis and molecular cytogenetic characterization of a chromosome 1q42.3-q44 deletion in a fetus associated with ventriculomegaly on prenatal ultrasound | Chen, Chih-Ping; TSANG-MING KO ; Wang, Liang-Kai; Chern, Schu-Rern; Wu, Peih-Shan; Chen, Shin-Wen; Wu, Fang-Tzu; Chen, Yun-Yi; Chen, Wen-Lin; Wang, Wayseen | Taiwanese journal of obstetrics & gynecology | 1 | 0 | |
2013 | Prenatal diagnosis and molecular cytogenetic characterization of a proximal deletion of 22q (22q11.2→q11.21) | Chen, Chih-Ping; TSANG-MING KO ; Su, Yi-Ning; Su, Jun-Wei; Chen, Yu-Ting; Lee, Chen-Chi; Chen, Li-Feng; Wang, Wayseen | Taiwanese journal of obstetrics & gynecology | 3 | 2 | |
2010 | Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 21 | Chen, Chih-Ping; Lin, Chyi-Chyang; TSANG-MING KO ; Tsai, Fuu-Jen; Chern, Schu-Rern; Lee, Chen-Chi; Chen, Yu-Ting; Wu, Pei-Chen; Wang, Wayseen | Taiwanese journal of obstetrics & gynecology | 6 | 8 | |
2010 | Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 8 | Chen, Chih-Ping; MING CHEN ; TSANG-MING KO ; Ma, Gwo-Chin; Tsai, Fuu-Jen; Tsai, Ming-Song; Wu, Pei-Chen; Lee, Chen-Chi; Chen, Li-Feng; Wang, Wayseen | Taiwanese journal of obstetrics & gynecology | 17 | 15 | |
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 | 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 | TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY | | | |
2017 | Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaicism for tetrasomy 18p at amniocentesis in a pregnancy with a favorable outcome | Chen, Chih-Ping; TSANG-MING KO ; Chen, Yi-Yung; Chern, Schu-Rern; Wu, Peih-Shan; Chen, Shin-Wen; Lai, Shih-Ting; Chuang, Tzu-Yun; Yang, Chien-Wen; Pan, Chen-Wen; Wang, Wayseen | Taiwanese journal of obstetrics & gynecology | 9 | 8 | |
2013 | Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 22 associated with cat eye syndrome | Chen, Chih-Ping; TSANG-MING KO ; Chen, Yi-Yung; Su, Jun-Wei; Wang, Wayseen | Gene | 10 | 10 | |
2019 | Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 3 | Chen, Chih-Ping; TSANG-MING KO ; Chen, Chen-Yu; Chern, Schu-Rern; Wu, Peih-Shan; Chen, Shin-Wen; Wu, Fang-Tzu; Pan, Chen-Wen; Wang, Wayseen | Taiwanese journal of obstetrics & gynecology | 0 | 0 | |
2016 | Prenatal diagnosis and molecular cytogenetic characterization of rec(10)dup(10p)inv(10)(p11.2q26.3) in a fetus associated with paternal pericentric inversion | Chen, Chih-Ping; TSANG-MING KO ; Su, Yi-Ning; Wang, Liang-Kai; Chern, Schu-Rern; Wu, Peih-Shan; Chen, Yen-Ni; Chen, Shin-Wen; Ko, Kevin; Lee, Chen-Chi; Chen, Li-Feng; Yang, Chien-Wen; Wang, Wayseen | Taiwanese journal of obstetrics & gynecology | 7 | 6 | |
2014 | Prenatal diagnosis and molecular cytogenetic characterization of chromosome 22q11.2 deletion syndrome associated with congenital heart defects | Kuo, Yu-Ling; Chen, Chih-Ping; Wang, Liang-Kai; TSANG-MING KO ; Chang, Tung-Yao; Chern, Schu-Rern; Wu, Peih-Shan; Chen, Yu-Ting; Chang, Shu-Yuan | Taiwanese journal of obstetrics & gynecology | 8 | 8 | |
2016 | Prenatal diagnosis of 22q11.2 deletion syndrome associated with right aortic arch, left ductus arteriosus, cardiomegaly, and pericardial effusion | Chen, Yen-Ni; Chen, Chih-Ping; TSANG-MING KO ; Wang, Liang-Kai; Wu, Pei-Chen; Chang, Tung-Yao; Wu, Peih-Shan; Yang, Chien-Wen; Wang, Wayseen | Taiwanese journal of obstetrics & gynecology | 3 | 4 | |
2018 | Prenatal diagnosis of a 0.7-Mb 17p13.3 microdeletion encompassing YWHAE and CRK but not PAFAH1B1 in a fetus without ultrasound abnormalities | Chen, Chih-Ping; TSANG-MING KO ; Wang, Liang-Kai; Chern, Schu-Rern; Wu, Peih-Shan; Chen, Shin-Wen; Lai, Shih-Ting; Chuang, Tzu-Yun; Yang, Chien-Wen; Lee, Chen-Chi; Wang, Wayseen | Taiwanese journal of obstetrics & gynecology | 7 | 5 | |
2020 | Prenatal diagnosis of a familial normal euchromatic variant of dup(15)(q11.2q11.2) in a pregnancy with a favorable outcome | Chen, Chih-Ping; TSANG-MING KO ; Huang, Jian-Pei; Chern, Schu-Rern; Wu, Peih-Shan; Chen, Shin-Wen; Wu, Fang-Tzu; Chen, Wen-Lin; Lee, Meng-Shan; Wang, Wayseen | Taiwanese journal of obstetrics & gynecology | 0 | 0 | |
2021 | Prenatal diagnosis of low-level mosaicism for a small supernumerary marker chromosome derived from chromosome 9q (9q13-q21.33) in a pregnancy with a favorable outcome, and cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes | Chen, Chih-Ping; Lo, Liang-Ming; TSANG-MING KO ; Chern, Schu-Rern; Wu, Peih-Shan; Chen, Shin-Wen; Wu, Fang-Tzu; Town, Dai-Dyi; Chen, Li-Feng; Chen, Yun-Yi; Wang, Wayseen | Taiwanese journal of obstetrics & gynecology | 7 | 5 | |
2016 | Prenatal diagnosis of low-level mosaicism for trisomy 2 associated with a favorable pregnancy outcome | Chen, Chih-Ping; TSANG-MING KO ; Chern, Schu-Rern; Wu, Peih-Shan; Chen, Yen-Ni; Chen, Shin-Wen; Chen, Li-Feng; Yang, Chien-Wen; Wang, Wayseen | Taiwanese journal of obstetrics & gynecology | 11 | 10 | |
2020 | Prenatal diagnosis of low-level mosaicism for trisomy 21 by amniocentesis in a pregnancy associated with maternal uniparental disomy of chromosome 21 in the fetus and a favorable outcome | Chen, Chih-Ping; TSANG-MING KO ; Chen, Yi-Yung; Chern, Schu-Rern; Wu, Peih-Shan; Chen, Shin-Wen; Wu, Fang-Tzu; Chen, Yun-Yi; Chen, Wen-Lin; Pan, Chen-Wen; Wang, Wayseen | Taiwanese journal of obstetrics & gynecology | 9 | 7 | |
2021 | Prenatal diagnosis of maternal uniparental disomy 16 associated with mosaic trisomy 16 at amniocentesis, and pericardial effusion and intrauterine growth restriction in the fetus | Chen, Chih-Ping; TSANG-MING KO ; Chern, Schu-Rern; Wu, Peih-Shan; Chen, Shin-Wen; Wu, Fang-Tzu; Chen, Yun-Yi; Town, Dai-Dyi; Chen, Li-Feng; Wang, Wayseen | Taiwanese journal of obstetrics & gynecology | 7 | 8 | |