馬偕醫學院機構典藏(Mackay Medical College Institutional Repository):Browse by Title

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 1051-1075 of 1689. (68 Page(s) Totally)
<< < 38 39 40 41 42 43 44 45 46 47 > >>
View [10|25|50] records per page

Date	Title	Authors
2013-10-01	Prenatal diagnosis and molecular cytogenetic characterization of a de novo pure distal 9p deletion and literature review	Chih-Ping Chen; Yi-Ning Su; Chen-Yu Chen; Schu-Rern Chern; Peih-Shan Wu; Jun-Wei Su; Chen-Chi Lee; Li-Feng Chen; Wayseen Wang
2011-06-01	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	Chih-Ping Chen; Yau-Kun Kuo; Yi-Ning Su; Schu-Rern Chern; Fuu-Jen Tsai; Pei-Chen Wu; Yu-Ting Chen; Dai-Dyi Town; Wayseen Wang
2011-09-01	Prenatal diagnosis and molecular cytogenetic characterization of a mosaic derivative Y chromosome derived from a de novo unbalanced reciprocal Yq;13q translocation	Chih-Ping Chen; Yi-Ning Su; Ming Chen; Jian-Pei Huang; Fuu-Jen Tsai; Pei-Chen Wu; Wen-Lin Chen; Wayseen Wang
2011-06-01	Prenatal diagnosis and molecular cytogenetic characterization of a small marker chromosome derived from Y chromosome	Chih-Ping Chen; Ming Chen; Gwo-Chin Ma; Shun-Ping Chang; Yi-Yung Chen; Pei-Chen Wu; Li-Feng Chen; Wayseen Wang
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

Showing items 1051-1075 of 1689. (68 Page(s) Totally)
<< < 38 39 40 41 42 43 44 45 46 47 > >>
View [10|25|50] records per page

Loading...