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Showing items 176-200 of 213  (9 Page(s) Totally)
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Institution Date Title Author
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)

Showing items 176-200 of 213  (9 Page(s) Totally)
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