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显示项目601-625 / 1754. (共71页)
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日期	题名	作者
2012-08-01	Effects of increased payment for ventilation tube insertion on decision making for paediatric otitis media with effusion	Mao-Che Wang; Chung-Kai Huang; Ying-Piao Wang; Ching-Wen Chien
2012-07-01	Ciliogenic RFX transcription factors regulate FGF1 gene promoter	Hsu YC; Kao CY; Chung YF; Chen MS; Chiu IM
2012-07-01	Human cytomegalovirus preferentially infects the neoplastic epithelium of colorectal cancer: A quantitative and histological analysis.	Chen HP, Jiang JK, Chen CY, Chou TY, Chen YC, Chang YT,; Lin SF, Chan CH, Yang CY, Lin CH, Lin JK, Cho WL, Chan YJ
2012-07-01	The HLA-B gene and Hashimoto disease in Han Chinese children: A case-control and family-based study	Huang CY, Chang TY, Chu CC, Lo FS, Ting WH, Lin CH, Wu; Lee YJ
2012-07-01	The Molecuolar Basis of Wound Healing Processes Induced by Lithospermi Radix: A Proteomics and Biochemical Analysis	Chia-Yen Hsiao; Tung-Hu Tsai; Kin-Fu Chak
2012-07-01	Efficacy of two different materials used in auricular acupressure on weight reduction and abdominal obesity	Ching-Hsiu Hsieh; Tsann-Jnn Su; Yu-Wen Fang; Pei-Hsuan Ch
2012-07-01	High Discovery Proportion and Fault Tolerance of Grid Information Service	Ming-Jeng Yang; Chin-Lin Kuo; Yao-Ming Yeh
2012-07-01	Leukocyte mitochondrial DNA alteration in systemic lupus erythematosus and its relevance to the susceptibility to lupus nephritis	Hui-Ting Lee; Chen-Sung Lin; Wei-Sheng Chen; Hsien-Tzung Liao; Chang-Youh Tsai; Yau-Huei Wei
2012-07-01	Pneumothorax, pneumomediastinum and pneumopericardium complications arising from a case of wisdom tooth extraction.	Chih-Hao Chen; Ho Chang; Hung-Chang Liu; Tzu-Ti Hung; Wen-Chien Huang
2012-07-01	The adequacy of single-incisional thoracoscopic surgery as a first-line endoscopic approach for the management of recurrent primary spontaneous pneumothorax: a retrospective study	Chih-Hao Chen; Shih-Yi Lee; Ho Chang; Hung-Chang Liu; Tzu-Ti Hung; Chao-Hung Chen
2012-06-01	馬偕醫學院圖書館電子報_第十期	馬偕醫學院圖書館編輯小組
2012-06-01	A de novo supernumerary marker chromosome derived from chromosome 9p (9p13.1->p23) associated with attention deficit and hyperactivity disorder	Chih-Ping Chen; Shuan-Pei Lin; Jun-Wei Su; Dai-Dyi Town; Wayseen Wang
2012-06-01	Identification of a COL1A2 mutation with a deletion spanning coding and intronic sequence in exon 19 and intron 19 in a fetus with osteogenesis imperfecta type II	Chih-Ping Chen; Yi-Ning Su; Fang-Yu Hung; Schu-Rern Chern; Jun-Wei Su; Wayseen Wang
2012-06-01	Identification of a deletion mutation in the short flanking repeat region of exon 44 of COL1A1 gene in a fetus with osteogenesis imperfecta type II	Chih-Ping Chen; Yi-Ning Su; Tung-Yao Chang; Schu-Rern Chern; Jun-Wei Su; Wayseen Wang
2012-06-01	Inv dup del(10q): Identification by fluorescence in situ hybridization and array comparative genomic hybridization in a fetus with two concurrent chromosomal rearrangements	Chih-Ping Chen; Ming Chen; Yi-Ning Su; Jian-Pei Huang; Gwo-Chin Ma; Shun-Ping Chang; Schu-Rern Chern; Yu-Ting Chen; Jun-Wei Su; Chen-Chi Lee; Dai-Dyi Town; Wayseen Wang
2012-06-01	Osteogenesis imperfecta type I: second-trimester diagnosis and incidental identification of a dominant COL1A1 deletion mutation in the asymptomatic father	Chih-Ping Chen; Yi-Ning Su; Tung-Yao Chang; Schu-Rern Chern; Chen-Yu Chen; Jun-Wei Su; Wayseen Wang
2012-06-01	Osteogenesis imperfecta type II: prenatal diagnosis and association with increased nuchal translucency and hypoechogenicity of the cranium	Chih-Ping Chen; Yi-Ning Su; Tung-Yao Chang; Ming-Chao Huang; Chun-Heng Pan; Schu-Rern Chern; Jun-Wei Su; Wayseen Wang
2012-06-01	Osteogenesis imperfecta type IV: prenatal molecular diagnosis and genetic counseling in a pregnancy carried to full term with favorable outcome	Chih-Ping Chen; Shuan-Pei Lin; Yi-Ning Su; Schu-Rern Chern; Ming-Huei Lin; Jun-Wei Su; 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
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
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
2012-06-01	Pure distal 11q deletion without additional genomic imbalances in a female infant with Jacobsen syndrome and a de novo unbalanced reciprocal translocation	Chih-Ping Chen; Shuan-Pei Lin; Chyong-Hsin Hsu; Schu-Rern Chern; Jun-Wei Su; Yen-Jiun Chen; Chen-Wen Pan; Wayseen Wang
2012-06-01	Pure distal 9p deletion in a female infant with cerebral palsy	Chih-Ping Chen; Shuan-Pei Lin; Yi-Ning Su; Jun-Wei Su; Schu-Rern Chern; Dai-Dyi Town; Wayseen Wang
2012-06-01	The HLA-DRB1 gene and Graves disease in Taiwanese children: a case-control and family-based study	Wu YL, Chang TY, Chu CC, Huang CY, Lo FS, Ting WH, Lin; Lee YJ

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