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Showing items 206-213 of 213  (5 Page(s) Totally)
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Institution Date Title Author
中國醫藥大學 2008-03 Prenatal sonographic and magnetic resonance imaging demonstration of a right midline arachnoid cyst associated with ventriculomegaly, colpocephaly, dilation of the third ventricle, absence of cavum septi pellucidum, agenesis of the corpus callosum and meg 陳持平(Chih-Ping Chen); (Tung-Yao Chang); (Jeng-Hsiu Hung); (Chen-Yu Chen); (Wayseen Wang)
中國醫藥大學 2008-03 Prenatal visualization of cebocephaly with a prominent nose in a second-trimester fetus with alobar holoprosencephaly and trisomy 13 陳持平(Chih-Ping Chen)*; (Jin-Chung Shih); (Chin-Yuan Tzen); (Schu-Rern Chern); (Chen-Ju Lin); (Wayseen Wang)
中國醫藥大學 2007-12 Genetic counseling of prenatally detected unbalanced t(Y;15)(q12;p13) 陳持平(Chih-Ping Chen); (Yi-Ning Su); (Chyi-Chyang Lin); (Yueh-Chun Li); (Lie-Jiau Hsieh); (Chen-Chi Lee); (Wayseen Wang)
中國醫藥大學 2006-02 Prenatal findings and molecular cytogenetic analyses of partial trisomy 12q (12q24.32->qter) and partial monosomy 21q22.2->qter 陳持平(Chih-Ping Chen); (Schu-Rern Chern); 林齊強(Chyi-Chyang Lin); (Tzu-Hao Wang); 李月君(Yueh-Chun Li); 謝麗嬌(Lie-Jiau Hsieh); (Chen-Chi Lee); (Hui-Min Hua); (Wayseen Wang)
中國醫藥大學 2005.04 A comparison of maternal age, sex ratio and associated major anomalies among fetal trisomy 18 cases with different cell division of error 陳持平(Chih-Ping Chen*); (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Ching-Yi Lin); (Yi-Hui Lin); (Wayseen Wang)
中國醫藥大學 2005.04 A comparison of maternal age, sex ratio and associated major anomalies among fetal trisomy 18 cases with different cell division of error 陳持平(Chih-Ping Chen*); (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Ching-Yi Lin); (Yi-Hui Lin); (Wayseen Wang)
中國醫藥大學 2004 Detection of a homozygous D645E mutation of the acid α-glucosidase gene and glycogen deposition in tissues in a second-trimester fetus with infantile glycogen storage disease type II 陳持平(Chih-Ping Chen); 林炫沛(Shuan-pei Lin); (Chin-Yuan Tzen); 蔡輔仁(Fuu-Jen Tsai); 胡務亮(Wuh-Liang Hwu); (Wayseen Wang)
中國醫藥大學 2004 Detection of a homozygous D645E mutation of the acid α-glucosidase gene and glycogen deposition in tissues in a second-trimester fetus with infantile glycogen storage disease type II 陳持平(Chih-Ping Chen); 林炫沛(Shuan-pei Lin); (Chin-Yuan Tzen); 蔡輔仁(Fuu-Jen Tsai); 胡務亮(Wuh-Liang Hwu); (Wayseen Wang)

Showing items 206-213 of 213  (5 Page(s) Totally)
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