English  |  正體中文  |  简体中文  |  Items with full text/Total items : 1621/1720
Visitors : 3663955      Online Users : 183
RC Version 5.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
Scope Adv. Search
LoginUploadHelpAboutAdminister

Jump to: [Chinese Items]   [0-9]   [ A B C D E F G H I J K L M N O P Q R S T U V W X Y Z ]
or enter the first few letters:   

Showing items 1076-1100 of 1718. (69 Page(s) Totally)
<< < 39 40 41 42 43 44 45 46 47 48 > >>
View [10|25|50] records per page
DateTitleAuthors
2010-06-01 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 Chih-Ping Chen; Chyi-Chyang Lin; Yi-Ning Su; Fuu-Jen Tsai; Yu-Ting Chen; Schu-Rern Chern; Chen-Chi Lee; Dai-Dyi Town; Li-Feng Chen; Pei-Chen Wu; Wayseen Wang
2010-09-01 Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 21 Chih-Ping Chen; Chyi-Chyang Lin; Tsang-Ming Ko; Fuu-Jen Tsai; Schu-Rern Chern; Chen-Chi Lee; Yu-Ting Chen; Pei-Chen Wu; Wayseen Wang
2010-09-01 Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 22 Chih-Ping Chen; Chyi-Chyang Lin; Yi-Ning Su; Fuu-Jen Tsai; Schu-Rern Chern; Chen-Chi Lee; Wen-Ling Chen; Li-Feng Chen; Pei-Chen Wu; Wayseen Wang
2010-12-01 Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 8 Chih-Ping Chen; Ming Chen; Tsang-Ming Ko; Gwo-Chin Ma; Fuu-Jen Tsai; Ming-Song Tsai; Pei-Chen Wu; Chen-Chi Lee; Li-Feng Chen; Wayseen Wang
2010-09-01 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 Chih-Ping Chen; Ming Chen; Yi-Ning Su; Fuu-Jen Tsai; Schu-Rern Chern; Chin-Yuan Hsu; Pei-Chen Wu; Dai-Dyi Town; Dong-Jay Lee; Gwo-Chin Ma; Wayseen Wang
2014-02-01 Prenatal diagnosis and molecular cytogenetic characterization of de novo pure partial trisomy 6p associated with microcephaly, craniosynostosis and abnormal maternal serum biochemistry Chih-Ping Chen; 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
2012-09-01 Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 2 Chih-Ping Chen; Ming Chen; Schu-Rern Chern; Peih-Shan Wu; Shun-Ping Chang; Dong-Jay Lee; Yu-Ting Chen; Li-Feng Chen; Jun-Wei Su; Alan Hwa-Ruey Hsieh; Alex Hwa-Jiun Hsieh; Wayseen Wang
2011-06-01 Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 4 Chih-Ping Chen; Ming Chen; Yi-Ning Su; Fuu-Jen Tsai; Schu-Rern Chern; Pei-Chen Wu; Wen-Lin Chen; Li-Feng Chen; Chen-Wen Pan; Wayseen Wang
2012-06-01 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 Chih-Ping Chen; Schu-Rern Chern; Tung-Yao Chang; Yi-Ning Su; Yi-Yung Chen; Jun-Wei Su; Wayseen Wang
2009-03-01 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 Chih-Ping Chen; Fuu-Jen Tsai; Schu-Rern Chern; Tung-Yao Chang; Chin-Yuan Hsu; Hung-Hung Lin; Wayseen Wang
2010-03-01 Prenatal diagnosis of a 4.9-Mb deletion of 10q11.21→q11.23 by array comparative genomic hybridization Chih-Ping Chen; Yi-Ning Su; Schu-Rern Chern; Fuu-Jen Tsai; Chin-Yuan Hsu; Chen-Chi Lee; Wayseen Wang
2011-12-01 Prenatal diagnosis of a de novo 17p13.1 microduplication in a fetus with ventriculomegaly and lissencephaly Chih-Ping Chen; Yi-Ning Su; Chin-Yuan Hsu; Yu-Peng Liu; Schu-Rern Chern; Li-Feng Chen; Wayseen Wang
2011-12-01 Prenatal diagnosis of a de novo interstitial deletion of chromosome 20q12 in a fetus with complex congenital heart defects, corpus callosum agenesis and intrauterine growth restriction Yi-Hui Lin; Chih-Ping Chen; Tze-Chien Chen; Chun-Sen Hsu; Szu-Yuan Chou; Shu-Chin Chien
2012-12-01 Prenatal diagnosis of an interstitial deletion of 10q (10q11.21->q21.1): array comparative genomic hybridization characterization and literature review Chih-Ping Chen; Yi-Ning Su; Schu-Rern Chern; Peih-Shan Wu; Jun-Wei Su; Dai-Dyi Town; Wayseen Wang
2007-09-01 Prenatal diagnosis of arachnoid cysts Chih-Ping Chen;
2007-06-01 Prenatal diagnosis of atypical facial clefting should alert amniotic band syndrome and prompt a search for associated amniotic bands and other structural anomalies Chih-Ping Chen;
2007-03-01 Prenatal diagnosis of concomitant gallbladder hydrops and pyelectasis with spontaneous resolution Chih-Ping Chen; Yu-Peng Liu; Shu-Chin Chien; Wayseen Wang
2008-05-01 Prenatal diagnosis of concomitant Wolf-Hirschhorn syndrome and split hand-foot malformation associated with partial monosomy 4p (4p16.1->er) and partial trisomy 10q (10q25.1->er) Chih-Ping Chen; Yann-Jang Chen; Schu-Rern Chern; Fuu-Jen Tsai; Tung-Yao Chang; Chen-Chi Lee; Dai-Dyi Town; Meng-Shan Lee; Wayseen Wang
2007-09-01 Prenatal diagnosis of Dandy-Walker malformation associated with distal limb deficiencies Chih-Ping Chen; Shu-Chin Chien; Schu-Rern Chern; Chin-Yuan Tzen; Wayseen Wang
2011-09-01 Prenatal diagnosis of directly transmitted benign 4q12-q13.1 quadruplication associated with tandem segmental amplifications of the LPHN3 gene Chih-Ping Chen; Yi-Ning Su; Yu-Ting Chen; Wen-Lin Chen; Lee James Hsu; Wayseen Wang
2007-10-01 Prenatal diagnosis of Fryns syndrome associated with a microdeletion at 8p23.1 Chih-Ping Chen; Tzu-Hao Wang; Yann-Jang Chen; Tung-Yao Chang; Yu-Peng Liu; Chin-Yuan Tzen; Schu-Rern Chern; Wayseen Wang
2007-09-01 Prenatal diagnosis of iniencephaly Chih-Ping Chen;
2007-04-01 Prenatal diagnosis of low-level mosaic tetrasomy 9p by amniocentesis Chih-Ping Chen; Tung-Yao Chang; Schu-Rern Chern; Chen-Chi Lee; Dai-Dyi Town; Meng-Shan Lee; Wayseen Wang
2011-09-01 Prenatal diagnosis of microvillus inclusion disease Chih-Ping Chen; Yi-Ning Su; Schu-Rern Chern; Pei-Chen Wu; Wayseen Wang
2009-12-01 Prenatal diagnosis of monosomy 17p (17p13.3→pter) associated with polyhydramnios, intrauterine growth restriction, ventriculomegaly and Miller-Dieker lissencephaly syndrome in a fetus Chin-Yi Lin; Chih-Ping Chen; Chiung-Ling Liau; Pen-Hua Su; Teng-Fu Tsao; Tung-Yao Chang; Wayseen Wang
Showing items 1076-1100 of 1718. (69 Page(s) Totally)
<< < 39 40 41 42 43 44 45 46 47 48 > >>
View [10|25|50] records per page

 


DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - Feedback