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"su jun wei"
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| 國立高雄應用科技大學 |
2017 |
應用AHP及FAHP於剛性路面施工品質評估
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蘇俊維; SU, JUN-WEI |
| 亞洲大學 |
201502 |
Detection of no isochromosome 20q by interphase fluorescence in situ hybridization on uncultured amniocytes in a pregnancy with mosaic isochromosome 20q in cultured amniocytes at amniocentesis
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Su, 陳持平*; Jun-Wei;Su, Jun-Wei;Ch, Schu-Rern;Chern, Schu-Rern;Kuo, Yu-Ling;Kuo, Yu-Ling;Wu, Peih-Shan;Wu, Peih-Shan;Le, Meng-Shan;Lee, Meng-Shan;Ya, Chien-Wen;Yang, Chien-Wen;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2015-02 |
Detection of no isochromosome 20q by interphase fluorescence in situ hybridization on uncultured amniocytes in a pregnancy with mosaic isochromosome 20q in cultured amniocytes at amniocentesis
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陳持平*;Su, Jun-Wei;Su, Jun-Wei;Ch, Schu-Rern;Chern, Schu-Rern;Kuo, Yu-Ling;Kuo, Yu-Ling;Wu, Peih-Shan;Wu, Peih-Shan;Le, Meng-Shan;Lee, Meng-Shan;Ya, Chien-Wen;Yang, Chien-Wen;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2015-02 |
Detection of no isochromosome 20q by interphase fluorescent in situ hybridization on uncultured amniocytes in a pregnancy with mosaic isochromosome 20q in cultured amniocytes at amniocentesis
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陳持平*;Su, Jun-Wei;Su, Jun-Wei;Ch, Schu-Rern;Chern, Schu-Rern;Kuo, Yu-Ling;Kuo, Yu-Ling;Wu, Peih-Shan;Wu, Peih-Shan;Le, Meng-Shan;Lee, Meng-Shan;Ya, Chien-Wen;Yang, Chien-Wen;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2014-03 |
A 1.37-Mb 12p11.22-p11.21 deletion coincident with a 367-kb 22q11.2 duplication detected by array comparative genomic hybridization in an adolescent girl with autism and difficulty in self-care of menstruation
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陳持平;Chen, Chih-Ping;Li, Shuan-Pei;Lin, Shuan-Pei;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Su, Jun-Wei;Su, Jun-Wei;Lee, Chen-Chi;Lee, Chen-Chi;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
201310 |
Mosaic small supernumerary marker chromosome 1 at amniocentesis: prenatal diagnosis, molecular genetic analysis and literature review
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陳持平;Chen, Chih-Ping;Chen, Ming;Chen, Ming;Su, Yi-Ning;Su, Yi-Ning;Hua, Jian-Pei;Huang, Jian-Pei;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Su, Jun-Wei;Su, Jun-Wei;Ch, Shun-Ping;Chang, Shun-Ping;Chen, Li-Feng;Chen, Li-Feng;Pan, Chen-Wen;Pan, Chen-Wen;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
201310 |
An interstitial deletion of 8q23.3-q24.22 associated with Langer-Giedion syndrome, Cornelia de Lange syndrome and epilepsy
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陳持平;Chen, Chih-Ping;Li, Shuan-Pei;Lin, Shuan-Pei;Liu, Yu-Peng;Liu, Yu-Peng;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Su, Jun-Wei;Su, Jun-Wei;Chen, Yu-Ting;Chen, Yu-Ting;Lee, Chen-Chi;Lee, Chen-Chi;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
201309 |
Chromosome 22q11.2 deletion syndrome: prenatal diagnosis, array comparative genomic hybridization characterization using uncultured amniocytes and literature review
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陳持平;Chen, Chih-Ping;Hua, Jian-Pei;Huang, Jian-Pei;Chen, Yi-Yung;Chen, Yi-Yung;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Su, Jun-Wei;Su, Jun-Wei;Chen, Yu-Ting;Chen, Yu-Ting;Chen, Wen-Lin;Chen, Wen-Lin;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
201309 |
Chromosome 18p deletion syndrome presenting holoprosencephaly and premaxillary agenesis: prenatal diagnosis and aCGH characterization using uncultured amniocytes
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陳持平;Chen, Chih-Ping;Hua, Jian-Pei;Huang, Jian-Pei;Chen, Yi-Yung;Chen, Yi-Yung;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Su, Jun-Wei;Su, Jun-Wei;Pan, Chen-Wen;Pan, Chen-Wen;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
201309 |
Prenatal diagnosis of mosaic trisomy 2 associated with abnormal maternal serum screening, oligohydramnios, intrauterine growth restriction, ventricular septal defect, preaxial polydactyly and facial dysmorphism
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陳持平;Chen, Chih-Ping;Chen, Yi-Yung;Chen, Yi-Yung;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Su, Jun-Wei;Su, Jun-Wei;Chen, Yu-Ting;Chen, Yu-Ting;Lee, Chen-Chi;Lee, Chen-Chi;Chen, Li-Feng;Li-Feng Chen, ;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
201309 |
De novo unbalanced translocation resulting in monosomy for distal 5p (5p14.1->pter) and 14q (14q32.31->qter) associated with fetal nuchal edema, microcephaly, intrauterine growth restriction and single umbilical artery: prenatal diagnosis and molecular
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陳持平;Chen, Chih-Ping;Fu, Chung-Hu;Fu, Chung-Hu;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Su, Jun-Wei;Su, Jun-Wei;Lee, Chen-Chi;Lee, Chen-Chi;Le, Meng-Shan;Lee, Meng-Shan;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
201309 |
Detection of maternal transmission of a splicing mutation in the TSC2 gene following prenatal diagnosis of fetal cardiac rhabdomyomas mimicking congenital cystic adenomatoid malformation of the lung and cerebral tubers and awareness of a family history of
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陳持平;Chen, Chih-Ping;Cha, Tung-Yao;Chang, Tung-Yao;Guo, Wan-Yuo;Guo, Wan-Yuo;Su, Yi-Ning;Su, Yi-Ning;Chen, Yi-Yung;Chen, Yi-Yung;Ch, Schu-Rern;Chern, Schu-Rern;Su, Jun-Wei;Su, Jun-Wei;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
201309 |
Rapid detection of K650E mutation in FGFR3 using uncultured amniocytes in a pregnancy affected with fetal cloverleaf skull, occipital pseudoencephalocele, ventriculomegaly, straight short femurs and thanatophoric dysplasia type II
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陳持平;Chen, Chih-Ping;Cha, Tung-Yao;Chang, Tung-Yao;Li, Ming-Huei;Lin, Ming-Huei;Ch, Schu-Rern;Chern, Schu-Rern;Su, Jun-Wei;Su, Jun-Wei;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
201309 |
Mosaic trisomy 14 at amniocentesis: prenatal diagnosis and literature review
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陳持平;Chen, Chih-Ping;Wang, Kuo-Gon;Wang, Kuo-Gon;Tsang-Ming, K;Ko, Tsang-Ming;Ch, Schu-Rern;Chern, Schu-Rern;Su, Jun-Wei;Su, Jun-Wei;Town, Dai-Dyi;Town, Dai-Dyi;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
201309 |
Application of interphase fluorescence in situ hybridization to uncultured amniocytes for differential diagnosis of pseudomosaicism from true mosaicism in mosaic isochromosome 20q detected at amniocentesis
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陳持平;Chen, Chih-Ping;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Su, Jun-Wei;Su, Jun-Wei;Chen, Yu-Ting;Chen, Yu-Ting;Chen, Li-Feng;Chen, Li-Feng;Pan, Chen-Wen;Pan, Chen-Wen;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
201309 |
Prenatal diagnosis of mosaic trisomy 12 associated with congenital overgrowth
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陳持平;Chen, Chih-Ping;Ch, Shing-Jyh;Chang, Shing-Jyh;Su, Jun-Wei;Su, Jun-Wei;Chen, Yu-Ting;Chen, Yu-Ting;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2013-10 |
An interstitial deletion of 8q23.3-q24.22 associated with Langer-Giedion syndrome, Cornelia de Lange syndrome and epilepsy
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陳持平;Chen, Chih-Ping;Li, Shuan-Pei;Lin, Shuan-Pei;Liu, Yu-Peng;Liu, Yu-Peng;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Su, Jun-Wei;Su, Jun-Wei;Chen, Yu-Ting;Chen, Yu-Ting;Lee, Chen-Chi;Lee, Chen-Chi;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2013-10 |
Mosaic small supernumerary marker chromosome 1 at amniocentesis: prenatal diagnosis, molecular genetic analysis and literature review
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陳持平;Chen, Chih-Ping;Chen, Ming;Chen, Ming;Su, Yi-Ning;Su, Yi-Ning;Hua, Jian-Pei;Huang, Jian-Pei;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Su, Jun-Wei;Su, Jun-Wei;Ch, Shun-Ping;Chang, Shun-Ping;Chen, Li-Feng;Chen, Li-Feng;Pan, Chen-Wen;Pan, Chen-Wen;Wang, Wayseen;Wang, Wayseen |
| 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
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陳持平;Chen, Chih-Ping;Tsang-Ming, K;Ko, Tsang-Ming;Chen, Yi-Yung;Su, Jun-Wei;Wang, Wayseen; |
| 亞洲大學 |
2013-07 |
6p21.2-p12.3 deletion detected by aCGH in an 8-year-old girl with cleidocranial dysplasia, psychomotor developmental delay and poor wound healing
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陳持平;Chen, Chih-Ping;Li, Shuan-Pei;Lin, Shuan-Pei;Liu, Yu-Peng;Liu, Yu-Peng;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;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2013-07 |
Cri-du-chat (5p-) syndrome presenting with cerebellar hypoplasia and hypospadias: prenatal diagnosis and aCGH characterization using uncultured amniocytes
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陳持平;Chen, Chih-Ping;Hu, Ming-Chao;Huang, Ming-Chao;Chen, Yi-Yung;Chen, Yi-Yung;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Chen, Yu-Ting;Chen, Yu-Ting;Su, Jun-Wei;Su, Jun-Wei;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2013-06 |
Ring chromosome 21 presenting with sacrococcygeal teratoma: prenatal diagnosis, molecular cytogenetic characterization and literature review
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陳持平;Chen, Chih-Ping;Cheng, Po-Jen;Cheng, Po-Jen;Shuenn-Dyh, C;Chang, Shuenn-Dyh;Lee, Yi-Xuan;Lee, Yi-Xuan;Sh, Jin-Chung;Shih, Jin-Chung;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Su, Jun-Wei;Su, Jun-Wei;Chen, Li-Feng;Chen, Li-Feng;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2013-06 |
A boy with cleft palate, hearing impairment, microcephaly, micrognathia and psychomotor retardation and a microdeletion in 6p25.3 involving the DUSP22 gene
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陳持平;Chen, Chih-Ping;Li, Shuan-Pei;Lin, Shuan-Pei;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Su, Jun-Wei;Su, Jun-Wei;Wang, Wayseen;Wang, Wayseen |
| 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
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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 |
| 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
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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 |
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