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"陳持平"

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Showing items 211-260 of 339  (7 Page(s) Totally)
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Institution Date Title Author
亞洲大學 2010-12 Partial trisomy 10q (10q25.1->qter) and partial monosomy 13q (13q34->qter) presenting with fetal pyelectasis: prenatal diagnosis and array comparative genomic hybridization characterization 陳持平;Chen, Chih-Ping;Su, Yi-Ning;Tsai, Fuu-Jen;Hsu, Chin-Yuan;Chern, Schu-Rern;Wu, Pei-Chen;Lee, Chen-Chi;Chen, Wen-Lin;Wang, Wayseen
亞洲大學 2010-12 Partial trisomy 16p (16p12.2->pter) and partial monosomy 22q (22q13.31->qter) presenting with fetal ascites and ventriculomegaly: prenatal diagnosis and array comparative genomic hybridization characterization 陳持平;Chen, Chih-Ping;Su, Yi-Ning;Young, Richard Shih-Hung;Tsai, Fuu-Jen;Wu, Pei-Chen;Chern, Schu-Rern;Town, Dai-Dyi;Pan, Chen-Wen;Wang, Wayseen
亞洲大學 2010-12 Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 8 陳持平;Chen, Chih-Ping;Chen, Ming;Ko, Tsang-Ming;Ma, Gwo-Chin;Tsai, Fuu-Jen;Tsai, Ming-Song;Wu, Pei-Chen;Lee, Chen-Chi;Che, Li-Feng;Wang, Wayseen
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
亞洲大學 2010-12 Prenatal sonographic features of Miller-Dieker syndrome 陳持平;Chen, Chih-Ping
亞洲大學 2010-12 Recurrent distal 16q duplication and terminal 22q deletion: prenatal diagnosis and genetic counseling 陳持平;Chen, Chih-Ping;Huang, Ming-Chao;Su, Yi-Ning;Tsai, Fuu-Jen;Wu, Pei-Chen;Lee, Chen-Chi;Town, Dai-Dyi;Pan, Chen-Wen;Wang, Wayseen
亞洲大學 2010-12 Stroke during pregnancy and puerperium: clinical perspectives ;Cheng, Shih-Jung;Chen, Pei-Hao;Chen, Lu-An;陳持平;Chen, Chih-Ping
亞洲大學 2010-09 A de novo 7.9 Mb deletion in 22q13.2->qter in a boy with autistic features, epilepsy, developmental delay atopic dermatitis and abnormal immunological findings 陳持平;Chen, Chih-Ping;Lin, Shuan-Pei;Chern, Schu-Rern;Tsai, Fuu-Jen;Wu, Pei-Chen;Lee, Chen-Chi;Chen, Yu-Ting;Wang, Wayseen
亞洲大學 2010-09 Mosaic ring chromosome 18, ring chromosome 18 duplication/deletion and disomy 18: perinatal findings and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridization 陳持平;Chen, Chih-Ping;Guo, Yung-Ting;Lin, Shuan-Pei;Su, Yi-Ning;Chen, Yann-Jang;Hseuh, Rui-Yuan;Lin, Yi-Hui;Wu, Pei-Chen;Lee, Chen-Chi;Chen, Yu-Ting;Wang, Wayseen
亞洲大學 2010-09 Mosaic trisomy 7 at amniocentesis: prenatal diagnosis and molecular genetic analyses 陳持平;Chen, Chih-Ping;Su, Yi-Ning;Chern, Schu-Rern;Hwu, Yu-Ming;Lin, Shuan-Pei;Hsu, Chyong-Hsin;Tsai, Fuu-Jen;Wang, Tao-Yeuan;Wu, Pei-Chen;Lee, Chen-Chi;Chen, Yu-Ting;Chen, Li-Feng;Wang, Wayseen
亞洲大學 2010-09 Mosaic trisomy 9 at amniocentesis: prenatal diagnosis and molecular genetic analyses 陳持平;Chen, Chih-Ping;Lin, Hsien-Ming;Su, Yi-Ning;Chern, Schu-Rern;Tsai, Fuu-Jen;Wu, Pei-Chen;Lee, Chen-Chi;Chen, Yu-Ting;Lee, Meng-Shan;Pan, Chen-Wen;Wang, Wayseen
亞洲大學 2010-09 Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 21 陳持平;Chen, Chih-Ping;Lin, Chyi-Chyang;Ko, Tsang-Ming;Tsai, Fuu-Jen;Chern, Schu-Rern;Lee, Chen-Chi;Chen, Yu-Ting;Wu, Pei-Chen;Wang, Wayseen
亞洲大學 2010-09 Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 22 陳持平;Chen, Chih-Ping;Lin, Chyi-Chyang;Su, Yi-Ning;Tsai, Fuu-Jen;Chern, Schu-Rern;Lee, Chen-Chi;Chen, Wen-Ling;Chen, Li-Feng;Wu, Pei-Chen;Wang, Wayseen
亞洲大學 2010-09 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 陳持平;Chen, Chih-Ping;Chen, Ming;Su, Yi-Ning;Tsai, Fuu-Jen;Chern, Schu-Rern;Hsu, Chin-Yuan;Wu, Pei-Chen;Town, Dai-Dyi;Lee, Dong-Jay;Ma, Gwo-Chin;Wang, Wayseen
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
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
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
亞洲大學 2010-07 Array-CGH detection of a de novo 2.8 Mb deletion in 2q24.2->q24.3 in a girl with autistic features and developmental delay 陳持平;Chen, Chih-Ping;Lin, Shuan-Pei;Chern, Schu-Rern;Chen, Yann-Jang;Tsai, Fuu-Jen;Wu, Pei-Chen;Wang, Wayseen
亞洲大學 2010-06 Apert syndrome associated with upper airway obstruction and gastroesophageal reflux presenting polyhydramnios in the third trimester 陳持平;Chen, Chih-Ping;Lin, Shuan-Pei;Su, Yi-Ning;Chen, Chen-Yu;Tsai, Fuu-Jen;Liu, Yu-Peng;Chern, Schu-Rern;Wu, Pei-Chen;Chen, Hsaio-En Cindy;Wang, Wayseen
亞洲大學 2010-06 Deletion 2q37.3->qter and duplication 15q24.3->qter characterized by array CGH in a girl with epilepsy and dysmorphic features 陳持平;Chen, Chih-Ping;Lin, Shuan-Pei;Chern, Schu-Rern;Tsai, Fuu-Jen;Wu, Pei-Chen;Lee, Chen-Chi;Chen, Li-Feng;Lee, Meng-Shan;Wang, Wayseen
亞洲大學 2010-06 Detection and comparison of the levels of cytomegalovirus DNA in amniotic fluid and fetal ascites in a second-trimester fetus with massive ascites, hyperechogenic bowel, ventriculomegaly and intrauterine growth restriction 陳持平;Chen, Chih-Ping;Chern, Schu-Rern;Wang, Tao-Yeuan;Tsai, Fuu-Jen;Lin, Hung-Hung;Wu, Pei-Chen;Wang, Wayseen
亞洲大學 2010-06 Detection of a balanced homologous acrocentric rearrangement rea(14q14q) and low-grade X-chromosome mosaicism in a couple with repeated pregnancy losses 陳持平;Chen, Chih-Ping;Chern, Schu-Rern;Wu, Chia-Hsun;Tsai, Fuu-Jen;Wu, Pei-Chen;Wang, Wayseen
亞洲大學 2010-06 Epicatechin gallate decreases the viability and subsequent embryonic development of mouse blastocysts Tu, Hsiao-Chen;陳持平;Chen, Chih-Ping;Chan, Wen-Hsiung
亞洲大學 2010-06 Fetal magnetic resonance imaging demonstration of central nervous system abnormalities and polydactyly associated with Joubert syndrome 陳持平;Chen, Chih-Ping;Su, Yi-Ning;Huang, Jon-Kway;Liu, Yu-Peng;Tsai, Fuu-Jen;Yang, Chun-Kuang;Huang, Jian-Pei;Chen, Chen-Yu;Wu, Pei-Chen;Wang, Wayseen
亞洲大學 2010-06 Mosaic tetrasomy 12p with discrepancy between fetal tissues and extraembryonic tissues: molecular analysis and possible mechanism of formation 陳持平;Chen, Chih-Ping;Su, Yi-Ning;Chern, Schu-Rern;Tsai, Fuu-Jen;Wu, Pei-Chen;Chen, Hsaio-En Cindy;Chiang, Shu-Shien;Wang, Wayseen
亞洲大學 2010-06 Pathophysiology of increased fetal nuchal translucency thickness 陳持平;Chen, Chih-Ping
亞洲大學 2010-06 Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 18 and associated with a reciprocal translocation involving chromosomes 17 and 18 陳持平;Chen, Chih-Ping;Lin, Chyi-Chyang;Su, Yi-Ning;Tsai, Fuu-Jen;Chen, Yu-Ting;Chern, Schu-Rern;Lee, Chen-Chi;Town, Dai-Dyi;Chen, Li-Feng;Wu, Pei-Chen;Wang, Wayseen
亞洲大學 2010-06 Prenatal sonographic features of Pallister-Killian syndrome 陳持平;Chen, Chih-Ping
亞洲大學 2010-03 Abnormally flat facial profile on two- and three-dimensional ultrasound and array comparative genomic hybridization for the diagnosis of Pallister-Killian syndrome 陳持平;Chen, Chih-Ping;Su, Yi-Ning;Hsu, Chin-Yuan;Tsai, Fuu-Jen;Chien, Shu-Chin;Chern, Schu-Rern;Lee, Meng-Shan;Wu, Pei-Chen;Chen, Hsaio-En Cindy;Wang, Wayseen
亞洲大學 2010-03 Prenatal diagnosis and genetic counseling of mosaic trisomy 13 陳持平;Chen, Chih-Ping
亞洲大學 2010-03 Prenatal diagnosis of a 4.9-Mb deletion of 10q11.21->q11.23 by array comparative genomic hybridization 陳持平;Chen, Chih-Ping;Su, Yi-Ning;Chern, Schu-Rern;Tsai, Fuu-Jen;Hsu, Chin-Yuan;Lee, Chen-Chi;Wang, Wayseen
亞洲大學 2010-03 Prenatal sonographic features of the fetuses in trisomy 13 pregnancies (IV) 陳持平;Chen, Chih-Ping
亞洲大學 2010-03 Rapid genome-wide aneuploidy diagnosis using uncultured amniocytes and array CGH in pregnancy with abnormal ultrasound findings detected in late second and third trimesters 陳持平;Chen, Chih-Ping;Su, Yi-Ning;Tsai, Fuu-Jen;Chern, Schu-Rern;Hsu, Chin-Yuan;Huang, Ming-Chao;Wang, Wayseen
亞洲大學 2010-03 Resectoscopic excision of the vaginal septum in a virgin with uterus didelphys and obstructed unilateral vagina ;Shih, Chao-Lan;Hung, Yao-Ching;陳持平;Chen, Chih-Ping;Chien, Shu-Chin;Lin, Wu-Chou
亞洲大學 2010-03 Second-trimester molecular prenatal diagnosis of sporadic Apert syndrome following sonographic findings of mild ventriculomegaly and clenched hands mimicking trisomy 18 陳持平;Chen, Chih-Ping;Su, Yi-Ning;Hsu, Chin-Yuan;Ling, Pei-Ying;Tsai, Fuu-Jen;Chern, Schu-Rern;Wu, Pei-Chen;Chen, Hsaio-En Cindy;Wang, Wayseen
亞洲大學 2010-03 Unbalanced and balanced heterologous Robertsonian translocations involving chromosome 21 at amniocentesis 陳持平;Chen, Chih-Ping;Chern, Schu-Rern;Wu, Pei-Chen;Tsai, Fuu-Jen;Lee, Chen-Chi;Town, Dai-Dyi;Chen, Wen-Lin;Chen, Li-Feng;Lee, Meng-Shan;Pan, Chen-Wen;Wang, Wayseen
亞洲大學 2010-02 Prenatal diagnosis of X-linked myotubular myopathy 陳持平;Chen, Chih-Ping;Lin, Shuan-Pei;Chern, Schu-Rern;Tsai, Fuu-Jen;Wang, Tao-Yeuan;Lin, Hung-Hung;Wang, Wayseen
國立臺灣大學 2010 Apert Syndrome Associated with Upper Airway Obstruction and Gastroesophageal Reflux Inducing Polyhydramnios in the Third Trimester 陳持平; 林炫沛; 蘇怡寧; 陳震宇; 蔡輔仁; 劉育朋; 陳樹人; 吳佩臻; 王偉信; CHEN, CHIH-PING; LIN, SHUAN-PEI; SU, YI-NING; CHEN, JEN-YEU; TSAI, FUU-JEN; LIU, YU-PENG; CHERN, SCHU-RERN; WU, PEI-CHEN; WANG, WAYSEEN
國立臺灣大學 2010 Fetal Magnetic Resonance Imaging Demonstration of Central Nervous System Abnormalities and Polydactyly Associated with Joubert Syndrome 陳持平; 蘇怡寧; 黃榮貴; 劉育朋; 蔡輔仁; 楊濬光; 黃建霈; 陳震宇; 吳佩臻; 王偉信; CHEN, CHIH-PING; SU, YI-NING; HUANG, JON-KWAY; LIU, YU-PENG; TSAI, FUU-JEN; YANG, CHUN-KUANG; HUANG, JIAN-PEI; CHEN, JEN-YEU; WU, PEI-CHEN; WANG, WAYSEEN
國立臺灣大學 2010 Mosaic Tetrasomy 12p with Discrepancy between Fetal Tissues and Extraembryonic Tissues: Molecular Analysis and Possible Mechanism of Formation 陳持平; 蘇怡寧; 陳樹人; 蔡輔仁; 吳佩臻; 王偉信; CHEN, CHIH-PING; SU, YI-NING; CHERN, SCHU-RERN; TSAI, FUU-JEN; WU, PEI-CHEN; WANG, WAYSEEN
國立臺灣大學 2010 Abnormally Rat Facial Profile on Two- and Three-Dimensional Ultrasound and Array Comparative Genomic Hybridization for the Diagnosis of Pallister- Killian Syndrome 陳持平; 蘇怡寧; 徐金源; 蔡輔仁; 簡淑卿; 陳樹人; 李孟珊; 吳佩臻; 王偉信; CHEN, CHIH-PING; SU, YI-NING; HSU, CHIN-YUAN; TSAI, FUU-JEN; CHIEN, SHU-CHIN; CHERN, SCHU-RERN; LEE, MENG-SHAN; WU, PEI-CHEN; WANG, WAYSEEN
國立臺灣大學 2010 Detection and Comparison of Cytomegalovirus DNA Levels in Amniotic Fluid and Fetal Ascites in a Second-Trimester Fetus with Massive Ascites, Hyperechogenic Bowel, Ventriculomegaly and Intrauterine Growth Restriction 陳持平; 蘇怡寧; 陳樹人; 王道遠; 蔡輔仁; 林虹宏; 吳佩臻; 王偉信; CHEN, CHIH-PING; SU, YI-NING; CHERN, SCHU-RERN; WANG, TAO-YEUAN; TSAI, FUU-JEN; LIN, HUNG-HUNG; WU, PEI-CHEN; WANG, WAYSEEN
國立臺灣大學 2010 Mosaic Ring Chromosome 18, Ring Chromosome 18 Duplication/Deletion and Disomy 18: Perinatal Findings and Molecular Cytogenetic Characterization by Fluorescence in Situ Hybridization and Array Comparative Genomic Hybridization 陳持平; 林炫沛; 蘇怡寧; 陳燕彰; 吳佩臻; 李貞姫; 王偉信; CHEN, CHIH-PING; LIN, SHUAN-PEI; SU, YI-NING; CHEN, YANN-JANG; WU, PEI-CHEN; LEE, CHEN-CHI; WANG, WAYSEEN
國立臺灣大學 2010 Mosaic Trisomy 7 at Amniocentesis: Prenatal Diagnosis and Molecular Genetic Analyses 陳持平; 蘇怡寧; 陳樹人; 林炫沛; 許瓊心; 蔡輔仁; 王道遠; 吳佩臻; 李貞姫; 陳麗鳳; 王偉信; CHEN, CHIH-PING; SU, YI-NING; CHERN, SCHU-RERN; LIN, SHUAN-PEI; HSU, CHYONG-HSIN; TSAI, FUU-JEN; WANG, TAO-YEUAN; WU, PEI-CHEN; LEE, CHEN-CHI; CHEN, LI-FENG; WANG, WAYSEEN
國立臺灣大學 2010 Mosaic Trisomy 9 at Amniocentesis: Prenatal Diagnosis and Molecular Genetic Analyses 陳持平; 蘇怡寧; 陳樹人; 蔡輔仁; 吳佩臻; 李貞姫; 李孟珊; 王偉信; CHEN, CHIH-PING; SU, YI-NING; CHERN, SCHU-RERN; TSAI, FUU-JEN; WU, PEI-CHEN; LEE, CHEN-CHI; LEE, MENG-SHAN; WANG, WAYSEEN
國立臺灣大學 2010 Prenatal Diagnosis and Molecular Cytogenetic Characterization of a Small Supernumerary Marker Chromosome Derived from Chromosome 18 and Associated with a Reciprocal Translocation Involving Chromosomes 17 and 18 陳持平; 林齊强; 蘇怡寧; 蔡輔仁; 陳樹人; 李貞姫; 吳佩臻; 王偉信; CHEN, CHIH-PING; LIN, CHYI-CHYANG; SU, YI-NING; TSAI, FUU-JEN; CHERN, SCHU-RERN; LEE, CHEN-CHI; WU, PEI-CHEN; WANG, WAYSEEN
國立臺灣大學 2010 Prenatal Diagnosis and Molecular Cytogenetic Characterization of a Small Supernumerary Marker Chromosome Derived from Chromosome 22 陳持平; 林齊强; 蘇怡寧; 蔡輔仁; 陳樹人; 李貞姫; 吳佩臻; 王偉信; CHEN, CHIH-PING; LIN, CHYI-CHYANG; SU, YI-NING; TSAI, FUU-JEN; CHERN, SCHU-RERN; LEE, CHEN-CHI; WU, PEI-CHEN; WANG, WAYSEEN
國立臺灣大學 2010 Prenatal Diagnosis of a 4.9-Mb Deletion of 10q11.21 -> Q11.23 by Array Comparative Genomic Hybridization 陳持平; 蘇怡寧; 陳樹人; 蔡輔仁; 徐金源; 李貞姫; 王偉信; CHEN, CHIH-PING; SU, YI-NING; CHERN, SCHU-RERN; TSAI, FUU-JEN; HSU, CHIN-YUAN; LEE, CHEN-CHI; 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
國立臺灣大學 2010 Rapid Genome-Wide Aneuploidy Diagnosis Using Uncultured Amniocytes and Array Comparative Genomic Hybridization in Pregnancy with Abnormal Ultrasound Findings Detected in Late Second and Third Trimesters 陳持平; 蘇怡寧; 蔡輔仁; 陳樹人; 徐金源; 黃閔照; 王偉信; CHEN, CHIH-PING; SU, YI-NING; TSAI, FUU-JEN; CHERN, SCHU-RERN; HSU, CHIN-YUAN; HUANG, MING-CHAO; WANG, WAYSEEN

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