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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
2017-04	Prenatal diagnosis and molecular cytogenetic characterization of concomitant familial small supernumerary marker chromosome derived from chromosome 4q ；4q11.1-q13.2 and 5q13.2 microdeletion with no apparent phenotypic abnormality	陳持平; Chih-Ping Chen; Schu-Rern Ch; Schu-Rern Chern; Peih-Shan Wu; Peih-Shan Wu; Yen-Ni Chen; Shin-Wen Che; Shin-Wen Chen; Chien-Wen Ya; Chien-Wen Yang; Chen-Chi Lee; Meng-Shan Le; Meng-Shan Lee
2016-04	Prenatal diagnosis and molecular cytogenetic characterization of de novo partial monosomy 3p (3p26.3->pter) and partial trisomy 16q (16q23.1->qter)	Wang；, 陳持平；Chih-Ping Chen；*；Fang-Yu Hung；Fang-Yu Hung；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；Wayseen Wang；Wayseen
2016-04	Prenatal diagnosis and molecular cytogenetic characterization of de novo partial monosomy 3p (3p26.3->pter) and partial trisomy 16q (16q23.1->qter)	陳持平; Chen, Chih-Ping; *; Hung, Fang-Yu; Hung, Fang-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; Lee, Chen-Chi; Lee, Chen-Chi; Wang, Wayseen; Wang, Wayseen
2016-04	Prenatal diagnosis and molecular cytogenetic characterization of de novo partial monosomy 3p (3p26.3->pter) and partial trisomy 16q (16q23.1->qter)	Chen)*, 陳持平(Chih-Ping; Hung), Fang-Yu Hung(Fang-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; Lee), Chen-Chi Lee(Chen-Chi; Wang), Wayseen Wang(Wayseen
2016-04	Prenatal diagnosis and molecular cytogenetic characterization of de novo partial monosomy 3p ;3p26.3->pter; and partial trisomy 16q ;16q23.1->qter;	陳持平; Chen, Chih-Ping; *; Hung, Fang-Yu; Hung, Fang-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; Lee, Chen-Chi; Lee, Chen-Chi; Wang, Wayseen; Wang, Wayseen
2013-03	Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 12q (12q24.21->qter) and partial monosomy 6q (6q27->qter) associated with coarctation of the aorta, ventriculomegaly and thickened nuchal fold	陳持平; Chen, Chih-Ping; Yi-Yung Chen; Schu-Rern Chern; Peih-Shan Wu; Jun-Wei Su; Yu-Ting Chen; Li-Feng Chen; Wayseen Wang
2010-09	Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 7p (7p15.3->pter) and partial monosomy 13q (13q33.3->qter) associated with Dandy-Walker malformation, abnormal skull development and microcephaly	陳持平; Chen, Chih-Ping; Chen, Ming; Su, Yi-Ning; Tsai, Fuu-Jen; Chern, Schu-Rern; Hsu, Chin-Yuan; Wu, Pei-Chen; Town, Dai-Dyi; Lee, Dong-Jay; Ma, Gwo-Chin; Wang, Wayseen
2014-02	Prenatal diagnosis and molecular cytogenetic characterization of de novo pure partial trisomy 6p associated with microcephaly, craniosynostosis and abnormal maternal serum biochemistry	陳持平; Chen, Chih-Ping; Ming Cheng; Chen-Yu Chen; Schu-Rern Chern; Peih-Shan Wu; Shun-Ping Chang; Yu-Ling Kuo; Wen-Lin Chen; Chen-Wen Pan; Wayseen Wang
2017-04	Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaic trisomy 12 at amniocentesis associated with a favorable pregnancy outcome	陳持平; Chih-Ping Chen; Chen-Ju Lin; Schu-Rern Ch; Schu-Rern Chern; Peih-Shan Wu; Yen-Ni Chen; Shin-Wen Che; Shin-Wen Chen; Chen-Wen Pan; Chien-Wen Ya; Chien-Wen Yang; Wayseen Wang
2017-12	Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaicism for tetrasomy 18p at amniocentesis in a pregnancy with a favorable outcome	陳持平; Chen, Chih-Ping; Tsang-Ming, K; Ko, Tsang-Ming; Chen, Yi-Yung; Ch, Schu-Rern; Chern, Schu-Rern; Che, Shin-Wen; Chen, Shin-Wen; La, Shih-Ting; Lai, Shih-Ting; Chua, Tzu-Yun; Chuang, Tzu-Yun; Ya, Chien-Wen; Yang, Chien-Wen; Pan, Chen-Wen; Wang, Wayseen
2016-04	Prenatal diagnosis and molecular cytogenetic characterization of low-level true mosaicism for trisomy 21 using uncultured amniocytes	陳持平; Chen, Chih-Ping; *; Wan, Yeou-Lih; Wang, Yeou-Lih; 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; Le, Meng-Shan; Lee, Meng-Shan; Ya, Chien-Wen; Yang, Chien-Wen; Wang, Wayseen; Wang, Wayseen
2016-04	Prenatal diagnosis and molecular cytogenetic characterization of low-level true mosaicism for trisomy 21 using uncultured amniocytes	Wang；, 陳持平；Chih-Ping Chen；*；Yeou-Lih Wan；Yeou-Lih Wang；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；Meng-Shan Le；Meng-Shan Lee；Chien-Wen Ya；Chien-Wen Yang；Wayseen Wang；Wayseen
2016-04	Prenatal diagnosis and molecular cytogenetic characterization of low-level true mosaicism for trisomy 21 using uncultured amniocytes	Chen)*, 陳持平(Chih-Ping; Wang), Yeou-Lih Wan(Yeou-Lih; 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; Lee), Meng-Shan Le(Meng-Shan; Yang), Chien-Wen Ya(Chien-Wen; Wang), Wayseen Wang(Wayseen
2013-10	Prenatal diagnosis and molecular cytogenetic characterization of mosaic ring chromosome 13	陳持平; Chen, Chih-Ping; Chin-Han Tsai; Schu-Rern Chern; Peih-Shan Wu; Jun-Wei Su; Chen-Chi Lee; Yu-Ting Chen; Wen-Lin Chen; Li-Feng Chen; Wayseen Wang
2013-10	Prenatal diagnosis and molecular cytogenetic characterization of mosaic ring chromosome 13	陳持平; Chen, Chih-Ping; Chin-Han Tsai; Schu-Rern Chern; Peih-Shan Wu; Jun-Wei Su; Chen-Chi Lee; Yu-Ting Chen; Wen-Lin Chen; Li-Feng Chen; Wayseen Wang
2017-06	Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 11	陳持平; Chih-Ping Chen; Ming Chen; Pu-Tsui Wang; Schu-Rern Ch; Schu-Rern Chern; Shin-Wen Che; Shin-Wen Chen; Shih-Ting La; Shih-Ting Lai; Peih-Shan Wu; Shun-Ping Ch; Shun-Ping Chang; Chen-Wen Pan; Wayseen Wang
2014-03	Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 15	陳持平; Chen, Chih-Ping; Chen, Ming; Chen, Ming; Su, Yi-Ning; Chern, Schu-Rern; Wu, Peih-Shan; Ch, Shun-Ping; Kuo, Yu-Ling; Chen, Wen-Lin; Wang, Wayseen
2017-08	Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 16	陳持平; Chih-Ping Chen; Tsang-Ming K; Tsang-Ming Ko; Schu-Rern Ch; Schu-Rern Chern; Shin-Wen Che; Shin-Wen Chen; Shih-Ting La; Shih-Ting Lai; Peih-Shan Wu; Chien-Wen Ya; Chien-Wen Yang; Chen-Wen Pan; Wayseen Wang
2017-04	Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 2	陳持平; Chih-Ping Chen; Ming Chen; Shun-Ping Ch; Shun-Ping Chang; Fang-Yu Hung; Meng-Ju Lee; Schu-Rern Ch; Schu-Rern Chern; Peih-Shan Wu; Yen-Ni Chen; Shin-Wen Chen; Chen-Chi Lee; Dai-Dyi Town; Meng-Shan Le; Meng-Shan Lee; Wen-Lin Chen; Wayseen Wang
2017-08	Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 21q11.2-q21.1 and a literature review	陳持平; Chih-Ping Chen; Ming Chen; Chia-Hsun Wu; Chen-Ju Lin; Schu-Rern Ch; Schu-Rern Chern; Peih-Shan Wu; Yen-Ni Chen; Shin-Wen Che; Shin-Wen Chen; Shun-Ping Ch; Shun-Ping Chang; Li-Feng Chen; Wayseen Wang
2013-09	Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 22 associated with cat eye syndrome	陳持平; Chen, Chih-Ping; Tsang-Ming, K; Ko, Tsang-Ming; Chen, Yi-Yung; Su, Jun-Wei; Wang, Wayseen
2012-09	Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 2	陳持平; Chen, Chih-Ping; Jun-Wei Su,; Alan Hwa-Ruey Hsieh,; Hsieh, Alex Hwa-Jiun; Wang, Wayseen
2011-06	Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 4	陳持平; Chen, Chih-Ping
2016-10	Prenatal diagnosis and molecular cytogenetic characterization of rec(10)dup(10p)inv(10)(p11.2q26.3) in a fetus associated with paternal pericentirc inversion	陳持平; Chen, Chih-Ping; *; Tsang-Ming, K; Ko, Tsang-Ming; Su, Yi-Ning; Su, Yi-Ning; Wa, Liang-Kai; Wang, Liang-Kai; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Chen, Yen-Ni; Chen, Yen-Ni; Che, Shin-Wen; Che, Shin-Wen; Town, Dai-Dyi; Town, Dai-Dyi; Chen, Li-Feng; Chen, Li-Feng; Ya, Chien-Wen; Yang, Chien-Wen; Wang, Wayseen; Wang, Wayseen
2012-06	Prenatal diagnosis and molecular genetic analysis of short rib-polydactyly syndrome type III (Verma-Naumoff) in a second-trimester fetus with a homozygous splice site mutation in intron 4 in the NEK1 gene	陳持平; Chen, Chih-Ping

Showing items 2351-2400 of 3308. (67 Page(s) Totally) << < 43 44 45 46 47 48 49 50 51 52 > >> View [10|25|50] records per page