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Showing items 891-900 of 3308. (331 Page(s) Totally) << < 85 86 87 88 89 90 91 92 93 94 > >> View [10|25|50] records per page

Date	Title	Authors
2016-12	Detection of a novel c.7106_7110delinsT heterozygous mutation in the FLNA gene in an asymptomatic mother with periventricular nodular heterotopia during prenatal genetic counseling	陳持平; Chen, Chih-Ping; *; Ch, Schu-Rern; Chern, Schu-Rern; Ch, Nan-Chang; Chiu, Nan-Chang; Liu, Yu-Peng; Liu, Yu-Peng; Chen, Yen-Ni; Chen, Yen-Ni; Che, Shin-Wen; Chen, Shin-Wen; Wang, Wayseen; Wang, Wayseen
2014-03	Detection of altered methylation status at 11p15 and 7q32 in placental mesenchymal dysplasia	陳持平; Chen, Chih-Ping; Su, Yi-Ning; Su, Yi-Ning; Li, Ming-Huei; Lin, Ming-Huei; Wa, Tao-Yeuan; Wang, Tao-Yeuan; Ch, Schu-Rern; Chern, Schu-Rern; Kuo, Yu-Ling; Kuo, Yu-Ling; Chen, Yu-Ting; Chen, Yu-Ting; Wang, Wayseen; Wang, Wayseen
2009-02	Detection of Conjugated Soy Metabolites in Urinary and Tissue Samples after Methanol Extraction	Chang, HC (Chang, Hebron C.); Han, J (Han, Jiayuan); Prior, RL (Prior, Ronald L.)
2009-01	Detection of Conjugated Soy Metabolites in Urinary and Tissue Samples after Methanol Extraction	張竣維; Hebron, C.Chang; Han, Jiayuan; Prior, Ronald L
2015-02	Detection of de novo secondary trisomy 13 due to isochromosome (13q;13q ; of paternal origin in a pregnancy with fetal cystic hygroma	; Ko, Tsang-Ming; Hu, Ming-Chao; Huang, Ming-Chao; Ch, Schu-Rern; Chern, Schu-Rern; Lin, Tan-Wei; Lin, Tan-Wei; Cha, Tung-Yao; Chang, Tung-Yao; Kuo, Yu-Ling; Kuo, Yu-Ling; Chen, Wen-Lin; Chen, Wen-Lin; Wang, Wayseen; Wang, Wayseen
	Detection of de novo secondary trisomy 13 due to isochromosome (13q;13q) of paternal origin in a pregnancy with fetal cystic hygroma	-
2015-02	Detection of de novo secondary trisomy 13 due to isochromosome (13q;13q) of paternal origin in a pregnancy with fetal cystic hygroma	Wang, 陳持平；Tsang-Ming K；Tsang-Ming Ko；Ming-Chao Hu；Ming-Chao Huang；Schu-Rern Ch；Schu-Rern Chern；Tan-Wei Lin；Tan-Wei Lin；Tung-Yao Cha；Tung-Yao Chang；Yu-Ling Kuo；Yu-Ling Kuo；Wen-Lin Chen；Wen-Lin Chen；Wayseen Wang；Wayseen
2015-02	Detection of de novo secondary trisomy 13 due to isochromosome (13q;13q) of paternal origin in a pregnancy with fetal cystic hygroma	陳持平*; Tsang-Ming, K; Ko, Tsang-Ming; Hu, Ming-Chao; Huang, Ming-Chao; Ch, Schu-Rern; Chern, Schu-Rern; Lin, Tan-Wei; Lin, Tan-Wei; Cha, Tung-Yao; Chang, Tung-Yao; Kuo, Yu-Ling; Kuo, Yu-Ling; Chen, Wen-Lin; Chen, Wen-Lin; Wang, Wayseen; Wang, Wayseen
	Detection of de novo secondary trisomy 13 due to isochromosome ;13q;13q) of paternal origin in a pregnancy with fetal cystic hygroma	陳持平*、Tsang-Ming, K; Ko, Tsang-Ming; Hu, Ming-Chao; Huang, Ming-Chao; Ch, Schu-Rern; Chern, Schu-Rern; Lin, Tan-Wei; Lin, Tan-Wei; Cha, Tung-Yao; Chang, Tung-Yao; Kuo, Yu-Ling; Kuo, Yu-Ling; Chen, Wen-Lin; Chen, Wen-Lin; Wang, Wayseen; Wang, Wayseen
2015-02	Detection of de novo secondary trisomy 13 due to isochromosome ;13q;13q; of paternal origin in a pregnancy with fetal cystic hygroma	陳持平; Tsang-Ming, K; Ko, Tsang-Ming; Hu, Ming-Chao; Huang, Ming-Chao; Ch, Schu-Rern; Chern, Schu-Rern; Lin, Tan-Wei; Lin, Tan-Wei; Cha, Tung-Yao; Chang, Tung-Yao; Kuo, Yu-Ling; Kuo, Yu-Ling; Chen, Wen-Lin; Chen, Wen-Lin; Wang, Wayseen; Wang, Wayseen

Showing items 891-900 of 3308. (331 Page(s) Totally) << < 85 86 87 88 89 90 91 92 93 94 > >> View [10|25|50] records per page