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顯示項目 682836-682845 / 2349128 (共234913頁)
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機構 日期 題名 作者
臺大學術典藏 2018-09-10T05:14:34Z Prenatal diagnosis by transabdominal chorionic villus sampling in the second and third trimesters Ko, T.-M.;Tseng, L.-H.;Hwa, H.-L.;Lee, T.-Y.;Chuang, S.-M.; LI-HUI TSENG; HSIAO-LIN HWA
臺大學術典藏 2022-03-10T07:58:57Z Prenatal diagnosis by transabdominal chorionic villus sampling in the second and third trimesters Ko T.-M.; LI-HUI TSENG; Hwa H.-L.; Lee T.-Y.; Chuang S.-M.
亞洲大學 2016-02 Prenatal diagnosis of 22q11.2 deletion syndrome associated with right aortic arch, left ductus arteriosus, cardiomegaly, and pericardial effusion Chen), Yen-Ni Chen(Yen-Ni;陳持平*;Ko), Tsang-Ming K(Tsang-Ming;Wang), Liang-Kai Wa(Liang-Kai;Wu), Pei-Chen Wu(Pei-Chen;Chang), Tung-Yao Cha(Tung-Yao;Wu), Peih-Shan Wu(Peih-Shan;Yang), Chien-Wen Ya(Chien-Wen;Wang), Wayseen Wang(Wayseen
亞洲大學 2016-02 Prenatal diagnosis of 22q11.2 deletion syndrome associated with right aortic arch, left ductus arteriosus, cardiomegaly, and pericardial effusion Chen, Yen-Ni;Chen, Yen-Ni;陳持平*;Tsang-Ming, K;Ko, Tsang-Ming;Wa, Liang-Kai;Wang, Liang-Kai;Wu, Pei-Chen;Wu, Pei-Chen;Cha, Tung-Yao;Chang, Tung-Yao;Wu, Peih-Shan;Wu, Peih-Shan;Ya, Chien-Wen;Yang, Chien-Wen;Wang, Wayseen;Wang, Wayseen
亞洲大學 2016-02 Prenatal diagnosis of 22q11.2 deletion syndrome associated with right aortic arch, left ductus arteriosus, cardiomegaly, and pericardial effusion Wang;, Yen-Ni Chen;Yen-Ni Chen;陳持平*;Tsang-Ming K;Tsang-Ming Ko;Liang-Kai Wa;Liang-Kai Wang;Pei-Chen Wu;Pei-Chen Wu;Tung-Yao Cha;Tung-Yao Chang;Peih-Shan Wu;Peih-Shan Wu;Chien-Wen Ya;Chien-Wen Yang;Wayseen Wang;Wayseen
臺大學術典藏 2020-02-14T02:50:41Z Prenatal diagnosis of 46, XX/47, XXY mosaicism: A case report Cheng W.?F.; Huang S.?C.; Ko T.?M.
亞洲大學 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 Chen, CP (Chen, Chih-Ping); Tsai, FJ (Tsai, Fuu-Jen); Chern, SR (Chern, Schu-Rern); Chang, TY (Chang, Tung-Yao); Hsu, CY (Hsu, Chin-Yuan); Lin, HH (Lin, Hung-Hung); Wang, W (Wang, Wayseen)
亞洲大學 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;Chen, Chih-Ping;Tsai, Fuu-Jen;Chern, Schu-Rern;Chang, Tung-Yao;Hsu, Chin-Yuan;Lin, Hung-Hung;Wang, Wayseen
中國醫藥大學 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)
亞洲大學 2018-02 Prenatal diagnosis of a 0.7-Mb 17p13.3 microdeletion encompassing YWHAE and CRK but not PAFAH1B1 in a fetus without ultrasound abnormalities 陳持平;Chen, Chih-Ping;*;Tsang-Ming, K;Ko, Tsang-Ming;Wa, Liang-Kai;Wang, Liang-Kai;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Che, Shin-Wen;Chen, Shin-Wen;La, Shih-Ting;Lai, Shih-Ting;Chua, Tzu-Yun;Chuang, Tzu-Yun;Ya, Chien-Wen;Yang, Chien-Wen;Lee, Chen-Chi;Lee, Chen-Chi;Wang, Wayseen;Wang, Wayseen

顯示項目 682836-682845 / 2349128 (共234913頁)
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