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Date	Title	Authors
2012-03	Prenatal diagnosis and genetic analysis of fetal akinesia deformation sequence and multiple pterygium syndrome associated with neuromuscular junction disorders: a review	陳持平; Chen, Chih-Ping
2010-03	Prenatal diagnosis and genetic counseling of mosaic trisomy 13	陳持平; Chen, Chih-Ping
2009-09	Prenatal diagnosis and molecular analysis of triploidy in a fetus with intrauterine growth restriction, relative macrocephaly and holoprosencephaly	陳持平; Chen, Chih-Ping; Chern, Schu-Rern; Tsai, Fuu-Jen; Hsu, Chin-Yuan; Ko, Kevin; Wang, Wayseen
2009-09	PRENATAL DIAGNOSIS AND MOLECULAR ANALYSIS OF TRIPLOIDY IN A FETUS WITH INTRAUTERINE GROWTH RESTRICTION, RELATIVE MACROCEPHALY AND HOLOPROSENCEPHALY	Chih-Ping Chen; Schu-Rern Chern; Fuu-Jen Tsai; Chin-Yuan Hsu; Kevin Ko; Wayseen Wang
2009-09	Prenatal diagnosis and molecular analysis of trisomy 13 mosaicism	陳持平; Chen, Chih-Ping; Chern, Schu-Rern; Tsai, Fuu-Jen; Lin, Hung-Hung; Pan, Chen-Wen; Wang, Wayseen
2009-09	PRENATAL DIAGNOSIS AND MOLECULAR ANALYSIS OF TRISOMY 13 MOSAICISM	Chih-Ping Chen; Schu-Rern Chern; Fuu-Jen Tsai; Hung-Hung Lin; Chen-Wen Pan; Wayseen Wang
2016-04	Prenatal diagnosis and molecular cytogenetic characterization of a de novo 4.858-Mb microdeletion in 15q14 associated with ACTC1 and MEIS2 haploinsufficiency and tetrology of Fallot	陳持平; Chen, Chih-Ping; *; Chen, Chen-Yu; Chen, Chen-Yu; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Chen, Yen-Ni; Chen, Yen-Ni; Che, Shin-Wen; Chen, Shin-Wen; Chen, Li-Feng; Chen, Li-Feng; Ya, Chien-Wen; Yang, Chien-Wen; Wang, Wayseen; Wang, Wayseen
2016-04	Prenatal diagnosis and molecular cytogenetic characterization of a de novo 4.858-Mb microdeletion in 15q14 associated with ACTC1 and MEIS2 haploinsufficiency and tetrology of Fallot	Wang；, 陳持平；Chih-Ping Chen；*；Chen-Yu Chen；Chen-Yu Chen；Schu-Rern Ch；Schu-Rern Chern；Peih-Shan Wu；Peih-Shan Wu；Yen-Ni Chen；Yen-Ni Chen；Shin-Wen Che；Shin-Wen Chen；Li-Feng Chen；Li-Feng Chen；Chien-Wen Ya；Chien-Wen Yang；Wayseen Wang；Wayseen
2016-04	Prenatal diagnosis and molecular cytogenetic characterization of a de novo 4.858-Mb microdeletion in 15q14 associated with ACTC1 and MEIS2 haploinsufficiency and tetrology of Fallot	Chen)*, 陳持平(Chih-Ping; Chen), Chen-Yu Chen(Chen-Yu; Chern), Schu-Rern Ch(Schu-Rern; Wu), Peih-Shan Wu(Peih-Shan; Chen), Yen-Ni Chen(Yen-Ni; Chen), Shin-Wen Che(Shin-Wen; Chen), Li-Feng Chen(Li-Feng; Yang), Chien-Wen Ya(Chien-Wen; Wang), Wayseen Wang(Wayseen
2013-06	Prenatal diagnosis and molecular cytogenetic characterization of a de novo interstitial deletion of 7q (7q22.1->q31.1)	陳持平; Chen, Chih-Ping; Shing-Jyh Chang; Schu-Rern Chern; Peih-Shan Wu; Yu-Ting Chen; Jun-Wei Su; Wen-Lin Chen; Wayseen Wang
2013	Prenatal diagnosis and molecular cytogenetic characterization of a de novo interstitial duplication of 14q (14q31.3->q32.12) associated with abnormal maternal serum biochemistry	陳持平; Chen, Chih-Ping; Kwui-Shuai Hwang; Her-Young Su; Shuan-Pei Lin; Yi-Ning Suk, Schu-Rern Chern; Jun-Wei Su; Yu-Ting Chen; Wen-Lin Chen; Wayseen Wang
2013-10	Prenatal diagnosis and molecular cytogenetic characterization of a de novo proximal interstitial deletion of chromosome 4p (4p15.2->p14)	陳持平; Chen, Chih-Ping; Meng-Ju Lee; Schu-Rern Chern; Peih-Shan Wu; Jun-Wei Su; Yu-Ting Chen; Meng-Shan Lee; Wayseen Wang
2013-10	Prenatal diagnosis and molecular cytogenetic characterization of a de novo proximal interstitial deletion of chromosome 4p (4p15.2->p14)	陳持平; Chen, Chih-Ping; Meng-Ju Lee; Schu-Rern Chern; Peih-Shan Wu; Jun-Wei Su; Yu-Ting Chen; Meng-Shan Lee; Wayseen Wang
2016-08	Prenatal diagnosis and molecular cytogenetic characterization of a de novo unbalanced reciprocal translocation of der(9)t(9;14)(p24.2;q32.11) associated with 9p terminal deletion and 14q distal duplication	陳持平; Chen, Chih-Ping; *; Lin, Chen-Ju; Lin, Chen-Ju; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Chen, Yen-Ni; Chen, Yen-Ni; Che, Shin-Wen; Chen, Shin-Wen; Lee, Chen-Chi; Lee, Chen-Chi; Chen, Li-Feng; Chen, Li-Feng; Ya, Chien-Wen; Yang, Chien-Wen; Wang, Wayseen; Wang, Wayseen
2016-08	Prenatal diagnosis and molecular cytogenetic characterization of a de novo unbalanced reciprocal translocation of der(9)t(9;14)(p24.2;q32.11) associated with 9p terminal deletion and 14q distal duplication	Wang；, 陳持平；Chih-Ping Chen；*；Chen-Ju Lin；Chen-Ju Lin；Schu-Rern Ch；Schu-Rern Chern；Peih-Shan Wu；Peih-Shan Wu；Yen-Ni Chen；Yen-Ni Chen；Shin-Wen Che；Shin-Wen Chen；Chen-Chi Lee；Chen-Chi Lee；Li-Feng Chen；Li-Feng Chen；Chien-Wen Ya；Chien-Wen Yang；Wayseen Wang；Wayseen
2011-06	Prenatal diagnosis and molecular cytogenetic characterization of a derivative chromosome der(18;18)(q10;q10)del(18)(q11.1q12.1)del(18)(q22.1q22.3) presenting as apparent isochromosome 18q in a fetus with holoprosencephaly	陳持平; Chen, Chih-Ping
2011-09	Prenatal diagnosis and molecular cytogenetic characterization of a mosaic derivative Y chromosome derived from a de novo unbalanced reciprocal Yq;13q translocation	陳持平; Chen, Chih-Ping
2013-03	Prenatal diagnosis and molecular cytogenetic characterization of a proximal deletion of 22q (22q11.2->q11.21)	陳持平; Chen, Chih-Ping; Tsang-Ming Ko; Yi-Ning Su; Jun-Wei Su; Yu-Ting Chen; Chen-Chi Lee; Li-Feng Chen; Wayseen Wang
2011-06	Prenatal diagnosis and molecular cytogenetic characterization of a small marker chromosome derived from Y chromosome	陳持平; Chen, Chih-Ping
2010-06	Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 18 and associated with a reciprocal translocation involving chromosomes 17 and 18	陳持平; Chen, Chih-Ping; Lin, Chyi-Chyang; Su, Yi-Ning; Tsai, Fuu-Jen; Chen, Yu-Ting; Chern, Schu-Rern; Lee, Chen-Chi; Town, Dai-Dyi; Chen, Li-Feng; Wu, Pei-Chen; Wang, Wayseen
2010-09	Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 21	陳持平; Chen, Chih-Ping; Lin, Chyi-Chyang; Ko, Tsang-Ming; Tsai, Fuu-Jen; Chern, Schu-Rern; Lee, Chen-Chi; Chen, Yu-Ting; Wu, Pei-Chen; Wang, Wayseen
2010-09	Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 22	陳持平; Chen, Chih-Ping; Lin, Chyi-Chyang; Su, Yi-Ning; Tsai, Fuu-Jen; Chern, Schu-Rern; Lee, Chen-Chi; Chen, Wen-Ling; Chen, Li-Feng; Wu, Pei-Chen; Wang, Wayseen
2010-12	Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 8	陳持平; Chen, Chih-Ping; Chen, Ming; Ko, Tsang-Ming; Ma, Gwo-Chin; Tsai, Fuu-Jen; Tsai, Ming-Song; Wu, Pei-Chen; Lee, Chen-Chi; Che, Li-Feng; Wang, Wayseen
2017-12	Prenatal diagnosis and molecular cytogenetic characterization of an interstitial deletion of 18q12.1-q12.3 encompassing DTNA, CELF4 and SETBP1	陳持平; Chen, Chih-Ping; Hs, Chih-Heng; Hsieh, Chih-Heng; Ch, Schu-Rern; Chern, Schu-Rern; 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; Wang, Wayseen
2014-06	Prenatal diagnosis and molecular cytogenetic characterization of chromosome 22q11.2 deletion syndrome associated with congenital heart defects	Yu-Ling Kuo; Chih-Ping Chen; Liang-Kai Wang; Tsang-Ming Ko; Tung-Yao Chang; Schu-Rern Chern; Peih-Shan Wu; Yu-Ting Chen; Shu-Yuan Chang

Showing items 2351-2375 of 3308. (133 Page(s) Totally) << < 90 91 92 93 94 95 96 97 98 99 > >> View [10|25|50] records per page