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Showing items 201-250 of 387. (8 Page(s) Totally)
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Date
Title
Authors
2009-01-01
PAL31 may play an important role as inflammatory modulator in the repair process of the spinal cord injury rat
Li-Fen Shen
;
Henrich Cheng
;
Ming-Chu Tsai
;
Huai-Sheng Kuo
;
Kin-Fu Chak
2011-06-01
Partial monosomy 13q (13q21.32→qter) and partial trisomy 8p (8p12→pter) presenting with anencephaly and increased nuchal translucency: array comparative genomic hybridization characterization
Chih-Ping Chen
;
Yi-Ning Su
;
Fuu-Jen Tsai
;
Ming-Huei Lin
;
Pei-Chen Wu
;
Schu-Rern Chern
;
Chen-Chi Lee
;
Chen-Wen Pan
;
Wayseen Wang
2012-09-01
Partial monosomy 3p (3p26.2->pter) and partial trisomy 5q (5q34->qter) in a girl with coarctation of the aorta, congenital heart defects, short stature, microcephaly and developmental delay
Chih-Ping Chen
;
Shuan-Pei Lin
;
Ming-Ren Chen
;
Yi-Ning Su
;
Schu-Rern Chern
;
Yu-Peng Liu
;
Jun-Wei Su
;
Meng-Shan Lee
;
Wayseen Wang
2012-06-01
Partial monosomy 9p (9p22.2->pter) and partial trisomy 18q (18q21.32->qter) in a female infant with anorectal malformations
Chih-Ping Chen
;
Hsien-Ming Lin
;
Cheung Leung
;
Shuan-Pei Lin
;
Yi-Ning Su
;
Jun-Wei Su
;
Yu-Ting Chen
;
Wayseen Wang
2010-12-01
Partial trisomy 10q (10q25.1→qter) and partial monosomy 13q (13q34→qter) presenting with fetal pyelectasis: prenatal diagnosis and array comparative genomic hybridization characterization
Chih-Ping Chen
;
Yi-Ning Su
;
Fuu-Jen Tsai
;
Schu-Rern Chern
;
Chin-Yuan Hsu
;
Pei-Chen Wu
;
Chen-Chi Lee
;
Wen-Lin Chen
;
Wayseen Wang
2010-12-01
Partial trisomy 16p (16p12.2→pter) and partial monosomy 22q (22q13.31→qter) presenting with fetal ascites and ventriculomegaly: prenatal diagnosis and array comparative genomic hybridization characterization
Chih-Ping Chen
;
Yi-Ning Su
;
Richard Shih-Hung Young
;
Fuu-Jen Tsai
;
Pei-Chen Wu
;
Schu-Rern Chern
;
Dai-Dyi Town
;
Chen-Wen Pan
;
Wayseen Wang
2012-12-01
Partial trisomy 1q (1q42.13->qter) and partial monosomy 6q (6q27->qter) in a girl with single median maxillary central incisor, dysgenesis of corpus callosum and developmental delay
Chih-Ping Chen
;
Shuan-Pei Lin
;
Yi-Ning Su
;
Schu-Rern Chern
;
Jun-Wei Su
;
Chen-Chi Lee
;
Wayseen Wang
2011-03-01
Pathological characterization of a malformed umbilical cord associated with body stalk anomaly
Chih-Ping Chen
;
Tao-Yeuan Wang
;
Pei-Chen Wu
;
Fuu-Jen Tsai
;
Wayseen Wang
2010-06-01
Pathophysiology of increased fetal nuchal translucency thickness
Chih-Ping Chen;
2012-04-01
Pericardial and thoracic peri-aortic adipose tissues contribute to systemic inflammation and calcified coronary atherosclerosis independent of body fat composition, anthropometric measures and traditional cardiovascular risks
Chun-Ho Yun
;
Tin-Yu Lin
;
Yih-Jer Wu
;
Chuan-Chuan Liu
;
Jen-Yuan Kuo
;
Hung-I. Yeh
;
Fei-Shih Yang
;
Su-Chiu Chen
;
Charles Jia-Yin Hou
;
Hiram G. Bezerra
;
Chung-Lieh Hung
;
Ricardo C. Cury
2007-09-01
Perinatal imaging findings of Galloway-Mowat syndrome
Chih-Ping Chen.
;
Shuan-Pei Lin
;
Jeng-Daw Tsai
;
Jon-Kway Huang
;
Jui-Lung Yen
;
Ching-Chang Tseng
;
Wayseen Wang
2012-04-01
Persistent cloaca presenting with a perineal cyst: prenatal ultrasound and magnetic resonance imaging findings
Chih-Ping Chen
;
Tung-Yao Chang
;
Chin-Yuan Hsu
;
Yu-Peng Liu
;
Fuu-Jen Tsai
;
Pei-Chen Wu
;
Wayseen Wang
2012-06-01
Phenotypic features associated with mosaic tetrasomy 9p in a 20-year-old female patient include autism spectrum disorder
Chih-Ping Chen
;
Shuan-Pei Lin
;
Jun-Wei Su
;
Meng-Shan Lee
;
Wayseen Wang
2012-06-01
Phenotypic features of pure 9p deletion in a male infant include cryptorchidism, congenital heart defects and postaxial polydactyly
Chih-Ping Chen
;
Shuan-Pei Lin
;
Ming-Ren Chen
;
Jun-Wei Su
;
Schu-Rern Chern
;
Yen-Jiun Chen
;
Meng-Shan Lee
;
Wayseen Wang
2008-01-01
A pilot study for screening blood donors in Taiwan by nucleic acid amplification technology: detecting occult hepatitis B virus infections and closing the serologic window period for hepatitis C virus.
Lei Li
;
Pei-Jer Chen
;
Ming-Hung Chen
;
Kin-Fu Chak
;
Kuo-Sin Lin
;
Su-Jen Lin Tsai
2010-03-01
Placenta percreta presenting as a pinhole uterine rupture and acute abdomen
Fang-Yu Hung
;
Pu-Tsui Wang
;
Shun-Long Weng
;
Chih-Ping Chen
2009-03-01
Placental abnormalities and preeclampsia in trisomy 13 pregnancies
Chih-Ping Chen.;
2010-12-01
Polysomnographic characteristics in patients with mucopolysaccharidoses
Hsiang-Yu Lin
;
Ming-Ren Chen
;
Ching-Chi Lin
;
Chih-Ping Chen
;
Dar-Shong Lin
;
Chih-Kuang Chuang
;
Dau-Ming Niu
;
Jui-Hung Chang
;
Hung-Chang Lee
;
Shuan-Pei Lin
2010-04-01
Posttranscriptional repression of the cel gene of the ColE7 operon by the RNA-binding protein CsrA of Escherichia coli.
Tsung-Yeh Yang
;
Yun-Min Sung
;
Guang-Sheng Lei
;
Tony Romeo
;
Kin-Fu Chak
2008-06-01
Prenatal 3-dimensional sonographic and MRI findings in omphalocele-exstrophy-imperforate anus-spinal defects complex
Chih-Ping Chen
;
Tung-Yao Chang
;
Yu-Peng Liu
;
Fuu-Jen Tsai
;
Shu-Chin Chien
;
Chien-Ming Tsao
;
Hsiao-Bai Yang
;
Wayseen Wang.
2011-06-01
Prenatal diagnosis and array comparative genomic hybridization characterization of a de novo interstitial deletion of chromosome 20p
Chih-Ping Chen
;
Yi-Ning Su
;
Schu-Rern Chern
;
Fuu-Jen Tsai
;
Pei-Chen Wu
;
Chen-Chi Lee
;
Wayseen Wang
2012-09-01
Prenatal diagnosis and array comparative genomic hybridization characterization of a de novo X;Y translocation
Chih-Ping Chen
;
Yi-Ning Su
;
Schu-Rern Chern
;
Jun-Wei Su
;
Yu-Ting Chen
;
Chen-Chi Lee
;
Wayseen Wang
2012-03-01
Prenatal diagnosis and genetic analysis of fetal akinesia deformation sequence and multiple pterygium syndrome associated with neuromuscular junction disorders: a review
Chih-Ping Chen;
2010-03-01
Prenatal diagnosis and genetic counseling for mosaic trisomy 13
Chih-Ping Chen;
2007-03-01
Prenatal diagnosis and genetic counseling of mucopolysaccharidosis type II (Hunter syndrome)
Chih-Ping Chen
;
Shuan-Pei Lin
;
Chin-Yuan Tzen
;
Wuh-Liang Hwu
;
Schu-Rern Chern
;
Chih-Kuang Chuang
;
Shu-Shien Chiang
;
Wayseen Wang
2009-09-01
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
2009-09-01
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
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
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 201-250 of 387. (8 Page(s) Totally)
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