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日期题名作者
2011-09-01 De novo duplication Xq22.1→q24 with a disruption of the NXF gene cluster in a mentally retarded woman with short stature and premature ovarian failure Chih-Ping Chen; Yi-Ning Su; Hung-Hung Lin; Schu-Rern Chern; Fuu-Jen Tsai; Pei-Chen Wu; Chen-Chi Lee; Yu-Ting Chen; Wayseen Wang
2014-01-01 De Novo MECP2 duplication derived from paternal germ line result in dysmorphism and developmental delay Dar-Shong Lin; Tzu-Po Chuang; Ming-Fu Chiang; Che-Sheng Ho; Chung-Der Hsiao; Yu-Wen Huang; Tsu-Yen Wu; Jer-Yuarn Wu; Yuan-Tsong Chen; Tsai-Chuan Chen; Ling-Hui Li.
2012-12-01 De novo satellited 2q associated with corpus callosum dysgenesis, short stature, mental retardation and developmental delay Chih-Ping Chen; Shuan-Pei Lin; Yuan-Ling Huang; Schu-Rern Chern; Yu-Peng Liu; Jun-Wei Su; Chen-Chi Lee; Wen-Lin Chen; Wayseen Wang
2012-06-01 A de novo supernumerary marker chromosome derived from chromosome 9p (9p13.1->p23) associated with attention deficit and hyperactivity disorder Chih-Ping Chen; Shuan-Pei Lin; Jun-Wei Su; Dai-Dyi Town; Wayseen Wang
2011-06-01 Decreased heat shock protein 27 expression and altered autophagy in human cells harboring A8344G mitochondrial DNA mutation Chin-Yi Chen; Hsueh-Fu Chen; Siao-Jhen Gi; Tang-Hao Chi; Che-Kun Cheng; Chi-Fu Hsu Yi-Shing Ma; Yau-Huei Wei; Chin-Shan Liu; Mingli Hsieh
2018-09-01 Deep brain stimulation modified autism-like deficits via the serotonin system in a valproic acid-induced rat model Han-Fang Wu; Yi-Ju Chen; Ming-Chia Chu; Ya-Ting Hsu; Ting-Yi Lu; I-Tuan Chen; Po See Chen; Hui-Ching Lin
2006-01-01 Deglycosylation of Na+/K+-ATPase causes the basolateral protein to undergo apical targeting in polarized hepatic cells Wei-Nan Lian; Tzu-Wei Wu; Ro-Lan Dao; Yann-Jang Chen; Chi-Hung Lin
2010-06-01 Deletion 2q37.3→qter and duplication 15q24.3→qter characterized by array CGH in a girl with epilepsy and dysmorphic features Chih-Ping Chen; Shuan-Pei Lin; Schu-Rern Chern; Fuu-Jen Tsai; Pei-Chen Wu; Chen-Chi Lee; Li-Feng Chen; Meng-Shan Lee; Wayseen Wang.
2003-02-01 Deletion of the C4-CYP21 repeat module leading to the formation of a chimeric CYP21P/CYP21 gene in a 9.3-kb fragment as a cause of steroid 21-hydroxylase deficiency Hsien-Hsiung Lee; Shwu-Fen Chang; Yann-Jinn Lee; Salmo Raskin; Shio-Jean Lin; Mei-Chyn Chao; Fu-Sung Lo; Ching-Yu Lin
2010-02-01 Deletion of the FHL2 Gene attenuates the formation of atherosclerotic lesions after a cholesterol-enriched diet Pao-Hsien Chu; Hung-I Yeh; Hsueh-Hua Wu; Ray-Ching Hong; Tzu-Fang Shiu; Chuen-Mao Yang

显示项目281-290 / 1254. (共126页)
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