瀏覽 依題名瀏覽 依日期瀏覽 依作者瀏覽 依資料類型瀏覽 子社群 中國藥學暨中藥資源學系暨碩博班 [450/600] 中獸醫碩士學位學程 [12/12] 中西醫結合研究所 [701/1265] 中醫學系暨碩博班 [1579/3217] 國際針灸碩士學位學程 [26/27] 學士後中醫學系 [126/609] 針灸研究所 [307/643] 中國醫學研究所 [407/887] 鄰近社群 人文與科技學院 [34/34] 校院出版品 [8671/8997] 牙醫學院 [239/915] 生命科學院 [952/1875] 醫學工程學院 [26/26] 中國醫藥大學 [187/486] 健康照護學院 [1952/4677] 公共衛生學院 [3364/6329] 北港附設醫院 [47/88] 台中附設醫院 [1721/5608] 校內其他單位 [51/58] 藥學院 [2167/5620] 通識教育中心 [209/583] 醫學院 [6284/12493] 最近上傳 Acupuncture Use Among Pregnant Pati... Mechanism Evidence in Acupuncture &... 耳針對六-羥基多巴胺造成帕金森氏症大鼠模式之神經保護作用 新冠肺炎感染後的腦霧穴位及量表文獻探討 比較敲筋按摩與按壓按摩對改善下背痛之效果評估 血液透析病人不寧腿症候群之針灸療效評估 濃縮中藥黃芩及黃芩?應用於犬黏液性二尖瓣性心臟病的療效評估 明代溫補學派醫家學術觀點與用藥探討 COVID-19 疫苗接種者的免疫反應與中醫體質的相關性研究 蒲公英萃取物減緩犬異位性皮膚炎機轉探討 —小鼠二硝基氯苯(DNCB)模... 上傳排行 資料載入中..... 下載排行 資料載入中.....

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顯示項目2876-2900 / 7244. (共290頁) << < 111 112 113 114 115 116 117 118 119 120 > >> 每頁顯示[10|25|50]項目

日期	題名	作者
2014-03	Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 15	陳持平(Chih-Ping Chen)*; (Ming Chen); (Yi-Ning Su); (Schu-Rern Chern); (Peih-Shan Wu); (Shun-Ping Chang); (Yu-Ling Kuo); (Wen-Lin Chen); (Wayseen Wang)
2012-09	Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 2	陳持平(Chih-Ping Chen)*; (Ming Chen); (Schu-Rern Chern); (Peih-Shan Wu); (Shun-Ping Chang); (Dong-Jay Lee); (Yu-Ting Chen); (Li-Feng Chen); (Jun-Wei Su,); (Alan Hwa-Ruey Hsieh); (Alex Hwa-Jiun Hsieh); (Wayseen Wang)
2012-06	Prenatal diagnosis and molecular genetic analysis of short rib-polydactyly syndrome type III (Verma-Naumoff) in a second-trimester fetus with a homozygous splice site mutation in intron 4 in the NEK1 gene	陳持平(Chih-Ping Chen)*; (Schu-Rern Chern); (Tung-Yao Chang); (Yi-Ning Su); (Yi-Yung Chen); (Jun-Wei Su); (Wayseen Wang)
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)
2010-03	Prenatal diagnosis of a 4.9-Mb deletion of 10q11.21->q11.23 by array comparative genomic hybridization	陳持平(Chih-Ping Chen)*; (Yi-Ning Su); (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Chin-Yuan Hsu); (Chen-Chi Lee); (Wayseen Wang)
2014-12	Prenatal diagnosis of a de novo 9p terminal chromosomal deletion in a fetus with major congenital anomalies	(Wen-Chien Hou); 陳持平(Chih-Ping Chen); (Kwei-Shuai Hwang); (Ying-Chieh Chen); (Yu-Ju Lai); (Chau-Yang Tien); (Her-Young Su)*
2011-12	Prenatal diagnosis of a de novo interstitial deletion of chromosome 20q12 in a fetus with complex congenital heart defects, corpus callosum agenesis and intrauterine growth restriction	(Yi-Hui Lin); 陳持平(Chih-Ping Chen)*; (Tze-Chien Chen); (Chun-Sen Hsu); (Szu-Yuan Chou); 簡淑錦(Shu-Chin Chien)
2006	Prenatal diagnosis of a micropenis in a male fetus with partial trisomy 12q (12q24.32->qter)and partial monosomy 21q(21q22.2->qter).	陳持平(Chen CP,); 林齊強(Lin CC,); 李月君(Li YC,); 謝麗嬌(Hsieh LJ,)
2013-03	Prenatal diagnosis of a missense mutation of c.2279G>A, Gly760Glu in exon 37 of COL1A2 in a fetus with familial osteogenesis imperfecta type IV and favorable outcome	陳持平(Chih-Ping Chen)*; (Shuan-Pei Lin); (Yi-Ning Su); (Schu-Rern Chern); (Jun-Wei Su); (Wayseen Wang)
2005	Prenatal diagnosis of an acardiac amorphous twin and the anomalous co-twin in a monoamniotic twin pregnancy	Chen, CP; Shih, JC; Chang, TY; Chern, SR; Lin, CY; Wang, WS; Tzen, CY
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)
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)
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)
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
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)

顯示項目2876-2900 / 7244. (共290頁) << < 111 112 113 114 115 116 117 118 119 120 > >> 每頁顯示[10|25|50]項目