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Showing items 146-195 of 201  (5 Page(s) Totally)
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Institution Date Title Author
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 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 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 2010-03 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 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 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 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
國立臺灣大學 2010 Second-Trimester Molecular Prenatal Diagnosis of Sporadic Apert Syndrome Following Sonographic Findings of Mild Ventriculomegaly and Clenched Hands Mimicking Trisomy 18 陳持平; 蘇怡寧; 徐金源; 蔡輔仁; 陳樹人; 吳佩臻; 王偉信; 林珮瑩; CHEN, CHIH-PING; SU, YI-NING; HSU, CHIN-YUAN; TSAI, FUU-JEN; CHERN, SCHU-RERN; WU, PEI-CHEN; WANG, WAYSEEN; LING, PEI-YING
國立臺灣大學 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 陳持平; 陳明; 蘇怡寧; 蔡輔仁; 陳樹人; 徐金源; 吳佩臻; 李東杰; 馬國欽; 王偉信; 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
亞洲大學 2009-12 Down syndrome due to unbalanced homologous acrocentric rearrangements and its recurrence in subsequent pregnancies: prenatal diagnosis by amniocentesis 陳持平;Chen, Chih-Ping;Chern, Schu-Rern;Tsai, Fuu-Jen;Wu, Pei-Chen;Lee, Chen-Chi;Chiang, Shu-Shien;Wang, Wayseen
亞洲大學 2009-12 Limb-body wall complex in one fetus of a dizygotic twin pregnancy obtained by egg donation, in vitro fertilization and embryo transfer: prenatal diagnosis and literature review 陳持平;Chen, Chih-Ping;Lee, Maw-Shuan;Tsai, Fuu-Jen;Huang, Ming-Chao;Chern, Schu-Rern;Wang, Wayseen
亞洲大學 2009-12 Prenatal diagnosis of a 22q11.2 microdeletion in a fetus with double-outlet right ventricle, pulmonary stenosis and a ventricular septal defect by array comparative genomic hybridization 陳持平;Chen, Chih-Ping;Su, Yi-Ning;Chang, Tung-Yao;Chern, Schu-Rern;Tsai, Fuu-Jen;Hwang, Jonathan Kwei;Wang, Wayseen
亞洲大學 2009-12 Prenatal diagnosis of monosomy 17p (17p13.3->pter) associated with polyhydramnios, intrauterine growth restriction, ventriculomegaly and Miller-Dieker lissencephaly syndrome in a fetus ;Lin, Chin-Yi;陳持平;Chen, Chih-Ping;Liau, Chiung-Ling;Su, Pen-Hua;Tsao, Teng-Fu;Chang, Tung-Yao;Wang, Wayseen
亞洲大學 2009-12 Prenatal diagnosis of terminal 2q deletion and distal 15q duplication by array comparative genomic hybridization using uncultured amniocytes 陳持平;Chen, Chih-Ping;Su, Yi-Ning;Tsai, Fuu-Jen;Lin, Hung-Hung;Chern, Schu-Rern;Lee, Meng-Shan;Hwang, Jonathan Kwei;Chen, Teresa Hsiao-Tien;Wang, Wayseen
亞洲大學 2009-12 Trisomy 13 mosaicism associated with cyclopia and cystic hygroma 陳持平;Chen, Chih-Ping;Chern, Schu-Rern;Tsai, Fuu-Jen;Wu, Pei-Chen;Lee, Chen-Chi;Wang, Wayseen
亞洲大學 2009-12 Unbalanced and balanced acrocentric rearrangements involving chromosomes other than 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 2009-09 Concomitant craniorachischisis and omphalocele in a male fetus: prenatal magnetic resonance imaging findings and literature review 陳持平;Chen, Chih-Ping;Liu, Yu-Peng;Tsai, Fuu-Jen;Chen, Chen-Yu;Lin, Hung-Hung;Wu, Pei-Chen;Wang, Wayseen
亞洲大學 2009-09 Prenatal diagnosis and molecular analysis of triploidy in a fetus with intrauterine growth restriction, relative macrocephaly and holoprosencephaly 陳持平;Chen, Chih-Ping;Chern, Schu-Rern;Tsai, Fuu-Jen;Hsu, Chin-Yuan;Ko, Kevin;Wang, Wayseen
亞洲大學 2009-09 Prenatal diagnosis and molecular analysis of trisomy 13 mosaicism 陳持平;Chen, Chih-Ping;Chern, Schu-Rern;Tsai, Fuu-Jen;Lin, Hung-Hung;Pan, Chen-Wen;Wang, Wayseen
亞洲大學 2009-09 Prenatal magnetic resonance imaging, ultrasound imaging findings and genetic analysis of concomitant rhabdomyomas and cerebral tuberous sclerosis 陳持平;Chen, Chih-Ping;Su, Yi-Ning;Chang, Tung-Yao;Liu, Yu-Peng;Tsai, Fuu-Jen;Hwang, Jonathan Kwei;Wang, Wayseen
亞洲大學 2009-03 PRENATAL DIAGNOSIS OF 46,XX,DER(13;21)(Q10;Q10),+21 AND TRANSIENT ABNORMAL MYELOPOIESIS IN A FETUS WITH HEPATOSPLENOMEGALY AND SPONTANEOUS RESOLUTION OF FETAL ASCITES 陳持平;Chen, Chih-Ping;Tsai, Fuu-Jen;Chern, Schu-Rern;Chang, Tung-Yao;Hsu, Chin-Yuan;Lin, Hung-Hung;Wang, Wayseen
亞洲大學 2009-01 A 12 Mb deletion of 6p24.1 -> pter in an 18-gestational-week fetus with orofacial clefting, the Dandy-Walker malformation and bilateral multicystic kidneys 陳持平;Chen, Chih-Ping;Tzen, Chin-Yuan;Chern, Schu-Rern;Tsai, Fuu-Jen;Hsu, Chin-Yuan;Lee, Chen-Chi;Lee, Meng-Shan;Pan, Chen-Wen;Wang, Wayseen
國立臺灣大學 2009 22q11.2 Microdeletion in a Fetus with Double-Outlet Right Ventricle, Pulmonary Stenosis and a Ventricular Septal Defect: Prenatal Diagnosis by Array Comparative Genomic Hybridization 陳持平; 蘇怡寧; 張東曜; 陳樹人; 蔡輔仁; 王偉信; CHEN, CHIH-PING; SU, YI-NING; CHANG, TUNG-YAO; CHERN, SCHU-RERN; TSAI, FUU-JEN; WANG, WAYSEEN
國立臺灣大學 2009 Terminal 2q Deletion and Distal 15q Duplication: Prenatal Diagnosis by Array Comparative Genomic Hybridization Using Uncultured Amniocytes 陳持平; 蘇怡寧; 蔡輔仁; 林虹宏; 陳樹人; 李孟珊; 王偉信; CHEN, CHIH-PING; SU, YI-NING; TSAI, FUU-JEN; LIN, HUNG-HUNG; CHERN, SCHU-RERN; LEE, MENG-SHAN; WANG, WAYSEEN
國立臺灣大學 2009 Prenatal Magnetic Resonance Imaging, Ultrasound Imaging Findings and Genetic Analysis of Concomitant Rhabdomyomas and Cerebral Tuberous Sclerosis 陳持平; 蘇怡寧; 張東曜; 劉育朋; 蔡輔仁; 王偉信; CHEN, CHIH-PING; SU, YI-NING; CHANG, TUNG-YAO; LIU, YU-PENG; TSAI, FUU-JEN; WANG, WAYSEEN
亞洲大學 2008-12 CONCOMITANT EXENCEPHALY AND LIMB DEFECTS ASSOCIATED WITH PENTALOGY OF CANTRELL 陳持平;Chen, Chih-Ping;Tzen, Chin-Yuan;Chen, Chen-Yu;Tsai, Fuu-Jen;Wang, Wayseen
亞洲大學 2008-12 LIMB-BODY WALL COMPLEX WITH CRANIOFACIAL DEFECTS AFTER OVARIAN STIMULATION 陳持平;Chen, Chih-Ping;Tsai, Fuu-Jen;Chen, Chen-Yu;Lin, Hung-Hung;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
亞洲大學 2008-03 CONCOMITANT OMPHALOCELE AND ANENCEPHALY ASSOCIATED WITH TRISOMY 18 AND ARTHROGRYPOSIS DIAGNOSED IN EARLY PREGNANCY 陳持平;Chen, Chih-Ping;Chang, Tung-Yao;Lin, Hung-Hung;Chern, Schu-Rern;Wang, Wayseen
亞洲大學 2008-03 PRENATAL VISUALIZATION OF CEBOCEPHALY WITH A PROMINENT NOSE IN A SECOND-TRIMESTER FETUS WITH ALOBAR HOLOPROSENCEPHALY AND TRISOMY 13 陳持平;Chen, Chih-Ping;Shih, Jin-Chung;Tzen, Chin-Yuan;Chern, Schu-Rern;Lin, Chen-Ju;Wang, Wayseen
國立臺灣大學 2008 Craniosynostosis and Congenital Tracheal Anomalies in an Infant with Pfeiffer Syndrome Carrying the W290c Fgfr2 Mutation 陳持平; 林炫沛; 蘇怡寧; 蔡輔仁; 王偉信; CHEN, CHIH-PING; LIN, SHUAN-PEI; SU, YI-NING; TSAI, FUU-JEN; WANG, WAYSEEN
國立臺灣大學 2008 Prenatal Visualization of Cebocephaly with a Prominent Nose in a Second- Trimester Fetus with Alobar Holoprosencephaly and Trisomy 13 陳持平; 施景中; 曾岐元; 陳樹人; 林珍如; 王偉信; CHEN, CHIH-PING; SHIH, JIN-CHUNG; TZEN, CHIN-YUAN; CHERN, SCHU-RERN; LIN, CHEN-JU; WANG, WAYSEEN
國立臺灣大學 2007 Genetic Counseling of Prenatally Detected Unbalancedt(Y;15)(Q12;P13) 陳持平; 蘇怡寧; 李貞姬; 王偉信; CHEN, CHIH-PING; SU, YI-NING; LEE, CHEN-CHI; WANG,WAYSEEN
國立臺灣大學 2006 A Cloverleaf Skull Associated with Crouzon Syndrome 陳持平; 林炫沛; 蘇怡寧; 王偉信; CHEN, CHIH-PING; LIN, SHUAN-PEI; SU, YI-NING; WANG, WAYSEEN

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