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中國醫藥大學機構典藏 China Medical University Repository, Taiwan > 依題名瀏覽

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日期	題名	作者
2012-12	Prenatal diagnosis of an interstitial deletion of 10q (10q11.21->q21.1): array comparative genomic hybridization characterization and literature review	陳持平(Chih-Ping Chen); (Yi-Ning Su); (Schu-Rern Chern); (Peih-Shan Wu); (Jun-Wei Su); (Dai-Dyi Town); (Wayseen Wang)*
2008-03-15	prenatal diagnosis of an XX male with the SRY gene on chromosome 3p	簡淑錦(Shu-Chin Chien)
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)*
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)*
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(Chih-Ping Chen); (Yi-Ning Su); (Shuan-Pei Lin); (Schu-Rern Chern); (Jun-Wei Su); (Yu-Ting Chen); (Meng-Shan Lee); (Wayseen Wang)*
1998	Prenatal diagnosis of Apert syndrome	Chang, CC; Tsai, FJ; Tsai, HD; Tsai, CH; Hsieh, YY; Lee, CC; Yang, TC; Wu, JY
2007-06	Prenatal diagnosis of atypical facial clefting should alert amniotic band syndrome and prompt a search for associated amniotic bands and other structural anomalies	陳持平(Chih-Ping Chen)*
2011-06	Prenatal diagnosis of cerebral tubers by magnetic resonance imaging following detection of cardiac rhabdomyomas by prenatal ultrasound in a fetus with a nonsense mutation in the TSC2 gene	陳持平(Chih-Ping Chen); (Yi-Ning Su); (Chin-Yuan Hsu); (Ming-Ren Chen); (Yu-Peng Liu); (Pei-Chen Wu); (Wayseen Wang)*
2015-12	Prenatal diagnosis of chromosome 8p23.1 microdeletion by array comparative genomic hybridization using uncultured amniocytes in a pregnancy associated with fetal partial corpus callosum agenesis and schizencephaly	陳持平(Chih-Ping Chen); (Cheng-Ran Peng); (Tung-Yao Chang); (Wan-Yuo Guo); (Yen-Ni Chen); (Peih-Shan Wu); (Dai-Dyi Town); (Wayseen Wang)*
2014-06-21	Prenatal diagnosis of coarctation of the aorta	裘品筠; 彭義欽; 莊子瑤; 張正成(Jeng-Sheng Chang); 裘品筠; 張正成(Jeng-Sheng Chang)
2005	Prenatal diagnosis of concomitant alobar holoprosencephaly and caudal regression syndrome associated with maternal diabetes	Chen, CP; Chen, CY; Lin, CY; Shaw, SW; Wang, WS; Tzen, CY
2007-05	Prenatal diagnosis of concomitant gallbladder hydrops and pyelectasis with spontaneous resolution.	陳持平(Chen CP)、劉玉鵬(Liu YP)、簡淑錦(Shu-Chin Chien)、王偉信(Wang W)*
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)
2007-09	Prenatal diagnosis of Dandy-Walker malformation associated with distal limb deficiencies	陳持平(Chih-Ping Chen)*
2013-12	Prenatal diagnosis of de novo cryptic microdeletions involving 5q23.1-q23.3 and 18q12.1-q12.3 by array CGH using uncultured amniocytes in a pregnancy with fetal interrupted aortic arch and atrial septal defect	陳持平(Chih-Ping Chen); (Ming-Chao Huang); (Yi-Yung Chen); (Schu-Rern Chern); (Peih-Shan Wu); (Yu-Ting Chen); (Jun-Wei Su); (Wayseen Wang)*
2005	Prenatal diagnosis of de novo partial trisomy 13q (13q22 -> qter) and partial monosomy 8p (8p23.3 -> pter) associated with holoprosencephaly, premaxillary agenesis, hexadactyly, and a hypoplastic left heart	Chen, CP; Chern, SR; Hsu, CY; Lee, CC; Lee, MS; Wang, WS
2005	Prenatal diagnosis of de novo proximal interstitial deletion of 9q and review of the literature of uncommon aneuploidies associated with increased nuchal translucency	Chen, CP; Chern, SR; Chang, TY; Chen, WL; Chen, LF; Wang, WS; Chen, HEC
2006	Prenatal diagnosis of de novo t(2;18;14) (q33.1;q12.2; q31.2),dup(5)(q34q34), del(7)(p21.1p21.1), and del(10) (q25.3q25.3) and a review of the prenatally ascertained de novo apparently balanced complex and multiple chromosomal rearrangements	陳持平(Chen CP,); (Chern SR,); (Lee CC,); 林齊強(Lin CC,); 李月君(Li YC,); 謝麗嬌(Hsieh LJ,); (Chen WL,); (Wang W.)
2011-09	Prenatal diagnosis of directly transmitted benign 4q12-q13.1 quadruplication associated with tandem segmental amplifications of the LPHN3 gene	陳持平(Chih-Ping Chen); (Yi-Ning Su); (Yu-Ting Chen); (Wen-Lin Chen); (Lee James Hsu); (Wayseen Wang)*
1999	Prenatal diagnosis of dyssegmental dysplasia - A case report	Hsieh, YY; Chang, CC; Tsai, HD; Lee, CC; Tsai, FJ; Tsai, CH
1999	Prenatal diagnosis of dyssegmental dysplasia - A case report	Hsieh, YY; Chang, CC; Tsai, HD; Lee, CC; Tsai, FJ; Tsai, CH
2011-01	Prenatal diagnosis of fetal hepatoblastoma with a good neonatal outcome: case report and narrative literature review	黃莉佳(Li-Chia Huang); 何銘(Ming- Ho); 張維君(Wei-Chun Chang); 陳慧毅(Huey-Yi Chen); 洪耀欽(Yao-Ching Hung); 邱燦宏(Tsan-Hung Chiu)*
2007-10	Prenatal diagnosis of Fryns syndrome associated with a microdeletion at 8p23.1	陳持平(Chih-Ping Chen)*
2014-03	Prenatal diagnosis of hypomethylation at KvDMR1 and Beckwith-Wiedemann syndrome in a pregnancy conceived by ICSI and IVF-ET	陳持平(Chih-Ping Chen); (Yi-Ning Su); (Shee-Uan Chen); (Tung-Yao Chang); (Pei-Chen Wu); (Schu-Rern Chern); (Peih-Shan Wu); (Yu-Ling Kuo); (Wayseen Wang)*
2011-09	Prenatal diagnosis of limb-body wall complex with craniofacial defects	陳持平(Chih-Ping Chen); (Yi-Yung Chen); (Jun-Wei Su); (Wayseen Wang)*
2005	Prenatal diagnosis of low-level mosaic trisomy 7 by amniocentesis	Chen, CP; Chern, SR; Chen, LF; Chen, WL; Wang, W
2006	Prenatal diagnosis of low-level mosaicism for a small XIST-negative supernumerary ring X chromosome in a nondysmorphic male fetus.	陳持平(Chen CP,); (Lin SP,); 林齊強(Lin CC,); 李月君(Li YC,); 謝麗嬌(Hsieh LJ,); (Chern SR,); (Lee CC,); (Chen LF,); (Wang W.)
2002	Prenatal diagnosis of lymphangiomas at unusual locations: report of three cases	何銘; 李建忠; 張穎宜; (戴金道); 蔡鴻德(Tsai,Horng-Der)
2011-09	Prenatal diagnosis of microvillus inclusion disease	陳持平(Chih-Ping Chen); (Yi-Ning Su); (Schu-Rern Chern); (Pei-Chen Wu); (Wayseen Wang)*
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)*
2009-10	Prenatal diagnosis of mos45,X/46,X,+mar in a fetus with normal male external genitalia and literature review	簡淑錦(Shu-Chin Chien); (Chih-Ping Chen); 林齊強(Chyi-Chyang Lin); 黃莉佳(Li-Chia Huang); (Cheng-Tiao Hsieh); 蔡輔仁(Fuu-Jen Tsai)*
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)*
2007-05	Prenatal diagnosis of mosaic ring chromosome 4	陳持平(Chih-Ping Chen); 徐金源(Chin-Yuan Hsu); 曾嶔元(Chin-Yuan Tzen); 李貞姬(Chen-Chi Lee); 陳文玲(Wen-Lin Chen); 陳麗鳳(Li-Feng Chen); 王偉信(Wayseen Wang)*
2003	Prenatal diagnosis of mosaic tetrasomy 10p associated with megacisterna magna, echogenic focus of left ventricle, umbilical cord cysts and distal arthrogryposis	Wu, YC; Yu, MT; Chen, LC; Chen, CL; Yang, ML
2012-12	Prenatal diagnosis of mosaic tetrasomy 18p	陳持平(Chih-Ping Chen); (Tsang-Ming Ko); (Yi-Ning Su); (Schu-Rern Chern); (Jun-Wei Su); (Yu-Ting Chen); (Dai-Dyi Town); (Wayseen Wang)*
2011-09	Prenatal diagnosis of mosaic trisomy 2: discrepancy between molecular cytogenetic analyses of uncultured amniocytes and karyotyping of cultured amniocytes in a pregnancy with severe fetal intrauterine growth restriction	陳持平(Chih-Ping Chen); (Yi-Ning Su); (Shin-Yu Lin); (Schu-Rern Chern); (Yu-Ting Chen); (Meng-Shan Lee); (Wayseen Wang)*
2011-09	Prenatal diagnosis of mosaic trisomy 8: clinical report and literature review	陳持平(Chih-Ping Chen); (Ming Chen); (Yi-Ju Pan); (Yi-Ning Su); (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Yu-Ting Chen); (Wayseen Wang)*
2001	Prenatal diagnosis of oculocutaneous albinism two mutations located at the same allele	Hsieh, YY; Wu, JY; Chang, CC; Tsai, FJ; Lee, CC; Tsai, HD; Tsai, CH
2001	Prenatal diagnosis of oculocutaneous albinism two mutations located at the same allele	Hsieh, YY; Wu, JY; Chang, CC; Tsai, FJ; Lee, CC; Tsai, HD; Tsai, CH
2010-12	Prenatal diagnosis of partial monosomy 1q (1q42.3->qter) associated with hydrocephalus and corpus callosum agenesis	陳持平(Chih-Ping Chen); (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Hung-Hung Lin); (Pei-Chen Wu); (Chen-Chi Lee); (Chen-Wen Pan); (Wayseen Wang)*
2005	Prenatal diagnosis of partial trisomy 10q (10q25.3 -> qter) and partial monosomy 18q (18q23 -> qter)	Chen, CP; Chern, SR; Chang, TY; Lee, CC; Chen, WL; Wang, W
2012-03	Prenatal diagnosis of partial trisomy 16p (16p12.2->pter) and partial monosomy 22q (22q13.31->qter) associated with increased nuchal translucency and abnormal maternal serum biochemistry in the first trimester	陳持平(Chih-Ping Chen); (Tsang-Ming Ko); (Yi-Ning Su); (Chin-Yuan Hsu); (Yi-Yung Chen); (Jun-Wei Su); (Wen-Lin Chen); (Wayseen Wang)*
2005	Prenatal diagnosis of partial trisomy 16q and distal 22q13 deletion associated with dolichocephaly and frontal bossing on second-trimester ultrasound	Chen, CP; Hsu, CY; Huang, JK; Lee, CC; Chen, WL; Wang, W
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)*
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(Chih-Ping Chen); (Yao-Lung Chang); (Schu-Rern Chern); (Peih-Shan Wu); (Jun-Wei Su); (Wen-Lin Chen); (Li-Feng Chen); (Wayseen Wang)*
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(Chih-Ping Chen); (Yu-Peng Liu); (Tung-Yao Chang); 蔡輔仁(Fuu-Jen Tsai); (Chen-Yu Chen); (Pei-Chen Wu); (Teresa Hsiao-Tien Chen); (Wayseen Wang)*
1999	The prenatal diagnosis of Pierre-Robin sequence	Hsieh, YY; Chang, CC; Tsai, HD; Yang, TC; Lee, CC; Tsai, CH
1999	The prenatal diagnosis of Pierre-Robin sequence	Hsieh, YY; Chang, CC; Tsai, HD; Yang, TC; Lee, CC; Tsai, CH
2013-03	Prenatal diagnosis of recurrent autosomal dominant osteogenesis imperfecta associated with unaffected parents and paternal gonadal mosaicism	陳持平(Chih-Ping Chen); (Shuan-Pei Lin); (Yi-Ning Su); (Schu-Rern Chern); (Jun-Wei Su); (Wayseen Wang)*
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(Chih-Ping Chen); (Yi-Ning Su); (Tung-Yao Chang); (Yu-Peng Liu); 蔡輔仁(Fuu-Jen Tsai); (Ming-Ren Chen); (Jonathan Kwei Hwang); (Teresa Hsiao-Tien Chen); (Wayseen Wang)*

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