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Showing items 171-213 of 213  (5 Page(s) Totally)
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Institution Date Title Author
中國醫藥大學 2010-02 Prenatal diagnosis of X-linked myotubular myopathy 陳持平(Chih-Ping Chen)*; (Shuan-Pei Lin); (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Tao-Yeuan Wang); (Hung-Hung Lin); (Wayseen Wang)
中國醫藥大學 2010-02 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(Chih-Ping Chen)*; (Chyi-Chyang Lin); (Yi-Ning Su); 蔡輔仁(Fuu-Jen Tsai); (Yu-Ting Chen); (Schu-Rern Chern); (Chen-Chi Lee); (Dai-Dyi Town); (Li-Feng Chen); (Pei-Chen Wu); (Wayseen Wang)
亞洲大學 2009-12 22q 11.2 Microdeletion in a Fetus With Double-outlet Right Ventricle, Pulmonary Stenosis and a Ventricular Septal Defect: Prenatal Diagnosis by Array Comparative Genomic Hybridization Chih-Ping Chen;Yi-Ning Su;Tung-Yao Chang;Schu-Rern Chern;Fuu-Jen Tsai;Jonathan Kwei Hwang;Wayseen Wang;
中國醫藥大學 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(Chih-Ping Chen)*; (Maw-Shuan Lee); 蔡輔仁(Fuu-Jen Tsai); (Ming-Chao Huang); (Schu-Rern Chern); (Wayseen Wang)
中國醫藥大學 2009-12 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(Chih-Ping Chen)*; (Yi-Ning Su); (Tung-Yao Chang); (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Jonathan Kwei Hwang); (Wayseen Wang)
中國醫藥大學 2009-12 Trisomy 13 mosaicism associated with cyclopia and cystic hygroma 陳持平(Chih-Ping Chen)*; (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Pei-Chen Wu); (Chen-Chi Lee); (Wayseen Wang)
中國醫藥大學 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 (Chin-Yi Lin); 陳持平(Chih-Ping Chen)*; (Chiung-Ling Liau); (Pen-Hua Su); (Teng-Fu Tsao); (Tung-Yao Chang); (Wayseen Wang)
中國醫藥大學 2009-12 Down syndrome due to unbalanced homologous acrocentric rearrangements and its recurrence in subsequent pregnancies: prenatal diagnosis by amniocentesis 陳持平(Chih-Ping Chen)*; (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Pei-Chen Wu); (Chen-Chi Lee); (Shu-Shien Chiang); (Wayseen Wang)
中國醫藥大學 2009-12 Unbalanced and balanced acrocentric rearrangements involving chromosomes other than chromosome 21 at amniocentesis 陳持平(Chih-Ping Chen)*; (Schu-Rern Chern); (Pei-Chen Wu); 蔡輔仁(Fuu-Jen Tsai); (Chen-Chi Lee); (Dai-Dyi Town); (Wen-Lin Chen); (Li-Feng Chen); (Meng-Shan Lee); (Chen-Wen Pan); (Wayseen Wang)
中國醫藥大學 2009-12 Prenatal diagnosis of terminal 2q deletion and distal 15q duplication by array comparative genomic hybridization using uncultured amniocytes 陳持平(Chih-Ping Chen)*; (Yi-Ning Su); 蔡輔仁(Fuu-Jen Tsai); (Hung-Hung Lin); (Schu-Rern Chern); (Meng-Shan Lee); (Jonathan Kwei Hwang); (Teresa Hsiao-Tien Chen); (Wayseen Wang)
亞洲大學 2009-09 PRENATAL DIAGNOSIS AND MOLECULAR ANALYSIS OF TRIPLOIDY IN A FETUS WITH INTRAUTERINE GROWTH RESTRICTION, RELATIVE MACROCEPHALY AND HOLOPROSENCEPHALY Chih-Ping Chen;Schu-Rern Chern;Fuu-Jen Tsai;Chin-Yuan Hsu;Kevin Ko;Wayseen Wang
亞洲大學 2009-09 PRENATAL DIAGNOSIS AND MOLECULAR ANALYSIS OF TRISOMY 13 MOSAICISM Chih-Ping Chen;Schu-Rern Chern;Fuu-Jen Tsai;Hung-Hung Lin;Chen-Wen Pan;Wayseen Wang
中國醫藥大學 2009-09 Pernatal diagnosis of partial trisomy 14q (14q31.1->qter) and partial monosomy 5p (5p13.2->pter) associated with polyhydramnios, a small thorax, short limbs, micropenis and brain malformations 陳持平(Chih-Ping Chen)*; (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Chen-Chi Lee); (Li-Feng Chen); (Wayseen Wang)
中國醫藥大學 2009-09 Concomitant craniorachischisis and omphalocele in a male fetus: prenatal magnetic resonance imaging findings and literature review 陳持平(Chih-Ping Chen)*; (Yu-Peng Liu); 蔡輔仁(Fuu-Jen Tsai); (Chen-Yu Chen); (Hung-Hung Lin); (Pei-Chen Wu); (Wayseen Wang)
中國醫藥大學 2009-09 Prenatal diagnosis of and molecular analysis of triploidy in a fetus with intrauterine growth restriction, relative macrocephaly and holoprosencephaly 陳持平(Chih-Ping Chen)*; (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Chin-Yuan Hsu); (Kevin Ko); (Wayseen Wang)
中國醫藥大學 2009-09 Prenatal diagnosis of and molecular analysis of trisomy 13 mosaicism 陳持平(Chih-Ping Chen)*; (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Hung-Hung Lin); (Chen-Wen Pan); (Wayseen Wang)
中國醫藥大學 2009-09 Prenatal magnetic resonance imaging, ultrasound imaging findings and genetic analysis of concomitant rhabdomyomas and cerebral tuberous sclerosis 陳持平(Chih-Ping Chen)*; (Yi-Ning Su); (Tung-Yao Chang); (Yu-Peng Liu); 蔡輔仁(Fuu-Jen Tsai); (Jonathan Kwei Hwang); (Wayseen Wang)
中國醫藥大學 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(Chih-Ping Chen); 蔡輔仁(Fuu-Jen Tsai); (Schu-Rern Chern); (Tung-Yao Chang); (Chin-Yuan Hsu); (Hung-Hung Lin); (Wayseen Wang)
中國醫藥大學 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(Chih-Ping Chen)*; (Chin-Yuan Tzen); (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Chin-Yuan Hsu); (Chen-Chi Lee); (Meng-Shan Lee); (Chen-Wen Pan); (Wayseen Wang)
中國醫藥大學 2008-12 Limb-body wall complex with craniofacial defects after ovarian stimulation 陳持平(Chih-Ping Chen)*; 蔡輔仁(Fuu-Jen Tsai); (Chen-Yu Chen); (Hung-Hung Lin); (Wayseen Wang)
中國醫藥大學 2008-12 Concomitant exencepahly and limb defects associated with pentalogy of Cantrell 陳持平(Chih-Ping Chen)*; (Chin-Yuan Tzen); (Chen-Yu Chen); 蔡輔仁(Fuu-Jen Tsai); (Wayseen Wang)
中國醫藥大學 2008-10 Characterization of a de novo unbalanced Y;autosome translocation in a 45,X mentally retarded male and literature review. 陳持平(Chih-Ping Chen)*; (Shuan-Pei Lin); 蔡輔仁(Fuu-Jen Tsai); (Tzu-Hao Wang); (Schu-Rern Chern); (Wayseen Wang)
中國醫藥大學 2008-10 Prenatal diagnosis of partial trisomy 3p (3p21->pter) and partial monosomy 11q (11q23->qter) associated with abnormal sonographic findings of alobar holoprosencephaly, orofacial clefts, pyelectasis and a unilateral duplex renal system 陳持平(Chih-Ping Chen)*; (Tzu-Hao Wang); (Chin-Yuan Hsu); (Chin-Yuan Tzen); (Chen-Chi. Lee); (Wayseen Wang)
中國醫藥大學 2008-09 Prenatal diagnosis of mosaic 1q31.3q32.1 trisomy associated with occipital encephalocele. 陳持平(Chih-Ping Chen)*; (Yann-Jang Chen); (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Hung-Hung Lin); (Chen-Chi Lee); (Wayseen Wang)
中國醫藥大學 2008-07 A 5.6 Mb deletion in 15q14 in a boy with speech and language disorder, cleft palate, epilepsy, a ventricular septal defect, mental retardation and developmental delay. 陳持平(Chih-Ping Chen)*; (Shuan-Pei Lin); 蔡輔仁(Fuu-Jen Tsai); (Schu-Rern Chern); (Chen-Chi Lee); (Wayseen Wang)
中國醫藥大學 2008-06 Kabuki syndrome in a female with mosaic 45,X/47,XXX and aortic coarctation. 陳持平(Chih-Ping Chen); (Shuan-Pei Lin); 蔡輔仁(Fuu-Jen Tsai); (Schu-Rern Chern); (Wayseen Wang)
中國醫藥大學 2008-06 Transient abnormal myelopoiesis of mosaic trisomy 21 presenting fetoplacental cytogenetic discrepancy, hepatosplenomegaly, oligohydramnios and abnormal hematological findings. 陳持平(Chih-Ping Chen); (Shuan-Pei Lin); 蔡輔仁(Fuu-Jen Tsai); (Hung-Hung Lin); (Schu-Rern Chern); (Chih-Kuang Chuang); (Chen-Chi Lee); (Wayseen Wang)
中國醫藥大學 2008-06 Craniosynostosis and congenital tracheal anomalies in an infant with Pfeiffer syndrome carrying the W290C FGFR2 mutation. 陳持平(Chih-Ping Chen); (Shuan-Pei Lin); (Yi-Ning Su); 簡淑錦(Shu-Chin Chien); 蔡輔仁(Fuu-Jen Tsai); (Wayseen Wang)
中國醫藥大學 2008-05 Prenatal diagnosis of concomitant Wolf-Hirschhorn syndrome and split hand foot malformation associated with partial monosomy 4p (4p16.1->pter) and partial trisomy 10q (10q25.1->qter) 陳持平(Chih-Ping Chen); (Yann-Jang Chen); (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Tung-Yao Chang); (Chen-Chi Lee); (Dai-Dyi Town); (Meng-Shan Lee); (Wayseen Wang)
中國醫藥大學 2008-04 NFkB2 gene duplication is associated with fetal pyelectasis in partial trisomy 10q (10q24.1->qter). 陳持平(Chih-Ping Chen); (Yann-Jang Chen); 蔡輔仁(Fuu-Jen Tsai); (Schu-Rern Chern); (Wayseen Wang)
亞洲大學 2008-03 PRENATAL SONOGRAPHIC AND MAGNETIC RESONANCE IMAGING DEMONSTRATION OF A RIGHT MIDLINE ARACHNOID CYST ASSOCIATED WITH VENTRICULOMEGALY, COLPOCEPHALY, DILATION OF THE THIRD VENTRICLE, ABSENCE OF CAVUM SEPTI PELLUCIDI, AGENESIS OF THE CORPUS CALLOSUM AND MEGA Cisterna Magna Chih-Ping Chen;Tung-Yao Chang;Jeng-Hsiu Hung;Chen-Yu Chen;Wayseen Wang
中國醫藥大學 2008-03 Prenatal evaluation of a giant blind ectopic ureter associated with a duplex kidney with magnetic resonance imaging. 陳持平(Chih-Ping Chen); (Yu-Peng Liu); (Jian-Pei Huang); (Tung-Yao Chang); 蔡輔仁(Fuu-Jen Tsai); (Jeng-DauTsai); (Jin-Cherng Sheu); (Wayseen Wang)
中國醫藥大學 2008-03 Triploidy and fetal holoprosencephaly 陳持平(Chih-Ping Chen); (Edison Hsieh); (Wayseen Wang)
中國醫藥大學 2008-03 Concomitant omphalocele and anencephaly associated with trisomy 18 and arthrogryposis diagnosed in early pregnancy 陳持平(Chih-Ping Chen)*; (Tung-Yao Chang); (Hung-Hung Lin); (Schu-Rern Chern); (Wayseen Wang)
中國醫藥大學 2008-03 Occipital encephalocele associated with iniencephaly mimicking an unilateral nuchal tumor on prenatal ultrasound. 陳持平(Chih-Ping Chen); (Yu-Ming Hwu); 蔡輔仁(Fuu-Jen Tsai); (Wayseen Wang)
中國醫藥大學 2008-03 Prenatal sonographic and magnetic resonance imaging demonstration of a right midline arachnoid cyst associated with ventriculomegaly, colpocephaly, dilation of the third ventricle, absence of cavum septi pellucidum, agenesis of the corpus callosum and meg 陳持平(Chih-Ping Chen); (Tung-Yao Chang); (Jeng-Hsiu Hung); (Chen-Yu Chen); (Wayseen Wang)
中國醫藥大學 2008-03 Prenatal visualization of cebocephaly with a prominent nose in a second-trimester fetus with alobar holoprosencephaly and trisomy 13 陳持平(Chih-Ping Chen)*; (Jin-Chung Shih); (Chin-Yuan Tzen); (Schu-Rern Chern); (Chen-Ju Lin); (Wayseen Wang)
中國醫藥大學 2007-12 Genetic counseling of prenatally detected unbalanced t(Y;15)(q12;p13) 陳持平(Chih-Ping Chen); (Yi-Ning Su); (Chyi-Chyang Lin); (Yueh-Chun Li); (Lie-Jiau Hsieh); (Chen-Chi Lee); (Wayseen Wang)
中國醫藥大學 2006-02 Prenatal findings and molecular cytogenetic analyses of partial trisomy 12q (12q24.32->qter) and partial monosomy 21q22.2->qter 陳持平(Chih-Ping Chen); (Schu-Rern Chern); 林齊強(Chyi-Chyang Lin); (Tzu-Hao Wang); 李月君(Yueh-Chun Li); 謝麗嬌(Lie-Jiau Hsieh); (Chen-Chi Lee); (Hui-Min Hua); (Wayseen Wang)
中國醫藥大學 2005.04 A comparison of maternal age, sex ratio and associated major anomalies among fetal trisomy 18 cases with different cell division of error 陳持平(Chih-Ping Chen*); (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Ching-Yi Lin); (Yi-Hui Lin); (Wayseen Wang)
中國醫藥大學 2005.04 A comparison of maternal age, sex ratio and associated major anomalies among fetal trisomy 18 cases with different cell division of error 陳持平(Chih-Ping Chen*); (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Ching-Yi Lin); (Yi-Hui Lin); (Wayseen Wang)
中國醫藥大學 2004 Detection of a homozygous D645E mutation of the acid α-glucosidase gene and glycogen deposition in tissues in a second-trimester fetus with infantile glycogen storage disease type II 陳持平(Chih-Ping Chen); 林炫沛(Shuan-pei Lin); (Chin-Yuan Tzen); 蔡輔仁(Fuu-Jen Tsai); 胡務亮(Wuh-Liang Hwu); (Wayseen Wang)
中國醫藥大學 2004 Detection of a homozygous D645E mutation of the acid α-glucosidase gene and glycogen deposition in tissues in a second-trimester fetus with infantile glycogen storage disease type II 陳持平(Chih-Ping Chen); 林炫沛(Shuan-pei Lin); (Chin-Yuan Tzen); 蔡輔仁(Fuu-Jen Tsai); 胡務亮(Wuh-Liang Hwu); (Wayseen Wang)

Showing items 171-213 of 213  (5 Page(s) Totally)
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