Items for Author "Su, Jun-Wei"
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Showing 30 items.
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| [生物科技學系] 期刊論文 |
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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 |
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 |
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| [生物科技學系] 期刊論文 |
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 |
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 |
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| [生物科技學系] 期刊論文 |
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 |
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 |
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| [生物科技學系] 期刊論文 |
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 |
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 |
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| [生物科技學系] 期刊論文 |
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Mosaic small supernumerary marker chromosome 1 at amniocentesis: prenatal diagnosis, molecular genetic analysis and literature review |
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 |
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| [生物科技學系] 期刊論文 |
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An interstitial deletion of 8q23.3-q24.22 associated with Langer-Giedion syndrome, Cornelia de Lange syndrome and epilepsy |
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 |
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| [生物科技學系] 期刊論文 |
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Chromosome 22q11.2 deletion syndrome: prenatal diagnosis, array comparative genomic hybridization characterization using uncultured amniocytes and literature review |
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 |
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| [生物科技學系] 期刊論文 |
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Chromosome 18p deletion syndrome presenting holoprosencephaly and premaxillary agenesis: prenatal diagnosis and aCGH characterization using uncultured amniocytes |
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 |
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| [生物科技學系] 期刊論文 |
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Prenatal diagnosis of mosaic trisomy 2 associated with abnormal maternal serum screening, oligohydramnios, intrauterine growth restriction, ventricular septal defect, preaxial polydactyly and facial dysmorphism |
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 |
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| [生物科技學系] 期刊論文 |
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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 |
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 |
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| [生物科技學系] 期刊論文 |
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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 |
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 |
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| [生物科技學系] 期刊論文 |
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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 |
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 |
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| [生物科技學系] 期刊論文 |
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Mosaic trisomy 14 at amniocentesis: prenatal diagnosis and literature review |
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 |
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| [生物科技學系] 期刊論文 |
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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 |
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 |
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| [生物科技學系] 期刊論文 |
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Prenatal diagnosis of mosaic trisomy 12 associated with congenital overgrowth |
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 |
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| [生物科技學系] 期刊論文 |
2013-10 |
An interstitial deletion of 8q23.3-q24.22 associated with Langer-Giedion syndrome, Cornelia de Lange syndrome and epilepsy |
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 |
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| [生物科技學系] 期刊論文 |
2013-10 |
Mosaic small supernumerary marker chromosome 1 at amniocentesis: prenatal diagnosis, molecular genetic analysis and literature review |
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 |
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| [生物科技學系] 期刊論文 |
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 |
陳持平; Chen, Chih-Ping; Tsang-Ming, K; Ko, Tsang-Ming; Chen, Yi-Yung; Su, Jun-Wei; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
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 |
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 |
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| [生物科技學系] 期刊論文 |
2013-07 |
Cri-du-chat (5p-) syndrome presenting with cerebellar hypoplasia and hypospadias: prenatal diagnosis and aCGH characterization using uncultured amniocytes |
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 |
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| [生物科技學系] 期刊論文 |
2013-06 |
Ring chromosome 21 presenting with sacrococcygeal teratoma: prenatal diagnosis, molecular cytogenetic characterization and literature review |
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 |
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| [生物科技學系] 期刊論文 |
2013-06 |
A boy with cleft palate, hearing impairment, microcephaly, micrognathia and psychomotor retardation and a microdeletion in 6p25.3 involving the DUSP22 gene |
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 |
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| [生物科技學系] 期刊論文 |
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 |
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| [生物科技學系] 期刊論文 |
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 |
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| [生物科技學系] 期刊論文 |
2013-03 |
Discrepancy in the trisomy mosaicism level between cultured amniocytes and uncultured amniocytes in prenatally detected mosaic trisomy 20 |
陳持平; Chen, Chih-Ping; Shuenn-Dyh, C; Chang, Shuenn-Dyh; Chueh, Ho-Yen; Chueh, Ho-Yen; Su, Yi-Ning; Su, Yi-Ning; Ch, Schu-Rern; Chern, Schu-Rern; Su, Jun-Wei; Su, Jun-Wei; Chen, Yu-Ting; Chen, Yu-Ting; Chen, Li-Feng; Chen, Li-Feng; Le, Meng-Shan; Lee, Meng-Shan; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2013-03 |
Mosaic trisomy 12 at amniocentesis: prenatal diagnosis and molecular genetic analysis |
陳持平; Chen, Chih-Ping; Su, Yi-Ning; Su, Yi-Ning; Su, Jun-Wei; Su, Jun-Wei; Ch, Schu-Rern; Chern, Schu-Rern; Chen, Yu-Ting; Chen, Yu-Ting; Chen, Li-Feng; Chen, Li-Feng; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2013-03 |
Placental mesenchymal dysplasia associated with antepartum hemorrhage, subchorionic hematoma and intrauterine growth restriction |
陳持平; Chen, Chih-Ping; Hs, Chin-Yuan; Hsu, Chin-Yuan; Su, Yi-Ning; Su, Yi-Ning; Wa, Tao-Yeuan; Wang, Tao-Yeuan; Chen, Yi-Yung; Chen, Yi-Yung; Ch, Schu-Rern; Chern, Schu-Rern; Su, Jun-Wei; Su, Jun-Wei; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2013-03 |
Prenatal diagnosis of a missense mutation of c.2279G>A, Gly760Glu in exon 37 of COL1A2 in a fetus with familial osteogenesis imperfecta type IV and favorable outcome |
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 |
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| [生物科技學系] 期刊論文 |
2013-03 |
Prenatal diagnosis of and molecular cytogenetic characterization of a de novo interstitial duplication of 11q (11q22.3->q23.3) associated with abnormal maternal serum biochemistry |
陳持平; Chen, Chih-Ping; Su, Yi-Ning; Su, Yi-Ning; Li, Shuan-Pei; Lin, Shuan-Pei; Ch, Schu-Rern; Chern, Schu-Rern; Su, Jun-Wei; Su, Jun-Wei; Chen, Yu-Ting; Chen, Yu-Ting; Le, Meng-Shan; Lee, Meng-Shan; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
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 |
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