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| 臺大學術典藏 |
2021-06-03T06:02:05Z |
Hereditary hearing impairment with cutaneous abnormalities
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Lee T.-L.; Lin P.-H.; PEI-LUNG CHEN; Hong J.-B.; Wu C.-C. |
| 臺大學術典藏 |
2021-06-03T06:02:04Z |
Genetic study of young-onset dementia using targeted gene panel sequencing in Taiwan
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Hsu J.-L.; Lin C.-H.; PEI-LUNG CHEN; Lin K.-J.; Chen T.-F. |
| 臺大學術典藏 |
2021-06-03T06:02:04Z |
Metabolic syndromes as important comorbidities in patients of inherited retinal degenerations: Experiences from the nationwide health database and a large hospital-based cohort
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Chiou G.-J.; Huang D.-S.; Hu F.-R.; Yang C.-M.; Yang C.-H.; Huang C.-W.; Lin J.-W.; Lin C.-W.; Ho T.-C.; Hsieh Y.-T.; Lai T.-T.; Chen H.-M.; PEI-LUNG CHEN; Hsiao C.K.; Chen T.-C. |
| 臺大學術典藏 |
2021-06-03T06:02:04Z |
Next-generation sequencing and bioinformatics to identify genetic causes of malignant hyperthermia
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Yeh H.-M.; Liao M.-H.; Chu C.-L.; Lin Y.-H.; Sun W.-Z.; Lai L.-P.; PEI-LUNG CHEN |
| 臺大學術典藏 |
2021-06-03T06:02:03Z |
Genetic characteristics and epidemiology of inherited retinal degeneration in Taiwan
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Chen T.-C.; Huang D.-S.; Lin C.-W.; Yang C.-H.; Yang C.-M.; Wang V.Y.; Lin J.-W.; Luo A.C.; Hu F.-R.; PEI-LUNG CHEN |
| 臺大學術典藏 |
2021-03-14T23:24:48Z |
Genetic study of young-onset dementia using targeted gene panel sequencing in Taiwan
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Hsu, Jung Lung; CHIN-HSIEN LIN; PEI-LUNG CHEN; Lin, Kun Ju; TA-FU CHEN |
| 臺大學術典藏 |
2021-03-14T23:24:35Z |
Genetic characteristics and epidemiology of inherited retinal degeneration in Taiwan
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TA-CHING CHEN; Huang, Ding Siang; Lin, Chao Wen; CHANG-HAO YANG; CHUNG-MAY YANG; Wang, Victoria Y.; JOU-WEI LIN; Luo, Allen Chilun; FUNG-RONG HU; PEI-LUNG CHEN |
| 臺大學術典藏 |
2021-03-14T23:24:34Z |
Metabolic syndromes as important comorbidities in patients of inherited retinal degenerations: Experiences from the nationwide health database and a large hospital-based cohort
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Chiou, Guann Jye; Huang, Ding Siang; FUNG-RONG HU; CHUNG-MAY YANG; CHANG-HAO YANG; Huang, Ching Wen; JOU-WEI LIN; Lin, Chao Wen; TZYY-CHANG HO; Hsieh, Yi Ting; Lai, Tso Ting; Chen, Ho Min; PEI-LUNG CHEN; CHUHSING KATE HSIAO; TA-CHING CHEN |
| 臺大學術典藏 |
2021-01-18T09:12:02Z |
Hereditary hearing impairment with cutaneous abnormalities
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Lee, Tung Lin; PEI-HSUAN LIN; PEI-LUNG CHEN; JIN-BON HONG; CHEN-CHI WU |
| 臺大學術典藏 |
2020-10-26T01:48:49Z |
Prediction Model for Audiological Outcomes in Patients with GJB2 Mutations
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Chen P.-Y.; Lin Y.-H.; Liu T.-C.; Lin Y.-H.; Tseng L.-H.; Yang T.-H.; PEI-LUNG CHEN; Wu C.-C.; Hsu C.-J. |
| 臺大學術典藏 |
2020-10-26T01:48:48Z |
Genotype-phenotype correlations of adult-onset PLA2G6-associated Neurodegeneration: Case series and literature review
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Chu Y.-T.;Lin H.-Y.;Pei-Lung Chen;Lin C.-H.; Chu Y.-T.; Lin H.-Y.; PEI-LUNG CHEN; Lin C.-H. |
| 臺大學術典藏 |
2020-10-26T01:48:48Z |
Next-generation sequencing and bioinformatics to identify genetic causes of malignant hyperthermia
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Liao M.-H.; Chu C.-L.; Lin Y.-H.; Sun W.-Z.; Lai L.-P.; PEI-LUNG CHEN; Yeh H.-M.; Yeh H.-M.;Liao M.-H.;Chu C.-L.;Lin Y.-H.;Sun W.-Z.;Lai L.-P.;Pei-Lung Chen |
| 臺大學術典藏 |
2020-10-26T01:48:48Z |
Cerebral microbleeds in autosomal dominant polycystic kidney disease
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Tsai L.-K.;Pei-Lung Chen;Tsai H.-H.;Chen Y.-F.;Wu P.-C.;Jeng J.-S.;Huang J.-W.;Chu T.-S.;Kao J.T.-W.; Tsai L.-K.; PEI-LUNG CHEN; Tsai H.-H.; Chen Y.-F.; Wu P.-C.; Jeng J.-S.; Huang J.-W.; Chu T.-S.; Kao J.T.-W. |
| 臺大學術典藏 |
2020-10-26T01:48:47Z |
The efficacy and safety of topical rapamycin–calcitriol for facial angiofibromas in patients with tuberous sclerosis complex: a prospective, double-blind, randomized clinical trial
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Pei-Lung Chen;Hong J.B.;Shen L.J.;Chen Y.T.;Wang S.J.;Liao Y.H.; PEI-LUNG CHEN; Hong J.B.; Shen L.J.; Chen Y.T.; Wang S.J.; Liao Y.H. |
| 臺大學術典藏 |
2020-10-26T01:48:46Z |
An integrative approach for pediatric auditory neuropathy spectrum disorders: revisiting etiologies and exploring the prognostic utility of auditory steady-state response
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Lin P.-H.;Hsu C.-J.;Lin Y.-H.;Lin Y.-H.;Yang S.-Y.;Yang T.-H.;Pei-Lung Chen;Wu C.-C.;Liu T.-C.; Lin P.-H.; Hsu C.-J.; Lin Y.-H.; Lin Y.-H.; Yang S.-Y.; Yang T.-H.; PEI-LUNG CHEN; Wu C.-C.; Liu T.-C. |
| 臺大學術典藏 |
2020-03-02T08:20:29Z |
Genetic determinants of antithyroid drug-induced agranulocytosis by human leukocyte antigen genotyping and genome-wide association study
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PEI-LUNG CHEN; Shih, Shyang-Rong; Wang, Pei-Wen; Lin, Ying-Chao; Chu, Chen-Chung; Lin, Jung-Hsin; Chen, Szu-Chi; Chang, Ching-Chung; Huang, Tien-Shang; Tsai, Keh Sung; Tseng, Fen-Yu; Wang, Chih-Yuan; Lu, Jin-Ying; Chiu, Wei-Yih; Chang, Chien-Ching; Chen, Yu-Hsuan; Chen, Yuan-Tsong; Fann, Cathy Shen-Jang; Yang, Wei-Shiung; Chang, Tien-Chun |
| 臺大學術典藏 |
2019-10-23T13:07:13Z |
Genetic Epidemiology and Clinical Features of Hereditary Hearing Impairment in the Taiwanese Population
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TIEN-CHEN LIU;CHEN-CHI WU;PEI-LUNG CHEN;Wu, Che Ming;Chen, Pey Yu;Lin, Yi Hsin;Lin, Yin Hung;Tsai, Cheng Yu;Erdenechuluun, Jargalkhuu;Hsu, Chuan Jen;Cheng, Yen Fu;Lee, Chee Yee;Lin, Pei Hsuan; Lin, Pei Hsuan; PEI-LUNG CHEN; Lee, Chee Yee; Cheng, Yen Fu; Hsu, Chuan Jen; Erdenechuluun, Jargalkhuu; Tsai, Cheng Yu; Lin, Yin Hung; CHEN-CHI WU; Lin, Yi Hsin; Chen, Pey Yu; TIEN-CHEN LIU; Wu, Che Ming |
| 臺大學術典藏 |
2019-08-27T05:32:21Z |
HSD3B1 gene polymorphism and female pattern hair loss in women with polycystic ovary syndrome
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Tu, Yi-An;Sung-Jan Lin;Pei-Lung Chen;Chou, Chia-Hung;Huang, Chu-Chun;Hong-Nerng Ho;Mei-Jou Chen; Tu, Yi-An; SUNG-JAN LIN; PEI-LUNG CHEN; Chou, Chia-Hung; Huang, Chu-Chun; HONG-NERNG HO; MEI-JOU CHEN |
| 臺大學術典藏 |
2019-08-27T05:29:52Z |
Distinctive genetic variation of long-segment Hirschsprung's disease in Taiwan
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Yang, Wendy;Chen, Szu-Chieh;Lai, Jin-Yao;Ming, Yung-Ching;Chen, Jeng-Chang;Pei-Lung Chen; Yang, Wendy; Chen, Szu-Chieh; Lai, Jin-Yao; Ming, Yung-Ching; Chen, Jeng-Chang; PEI-LUNG CHEN |
| 臺大學術典藏 |
2019-08-27T04:20:05Z |
A 49-Year-Old Man with Combined Myasthenia Gravis, Autoimmune Thyroiditis and IgG4 Orbitopathy
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Shan-Han Chang;Yung-Xin Tsai;Ta-Fu Chen;Wan-Chen Wu;Pei-Lung Chen;Jin-Ying Lu; Shan-Han Chang; Yung-Xin Tsai; TA-FU CHEN; WAN-CHEN WU; PEI-LUNG CHEN; Jin-Ying Lu |
| 臺大學術典藏 |
2019-08-27T04:13:16Z |
A stem-loop in the 3UTR of nos-2 is required for translational repression in oocytes
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Pei-Lung Chen; PEI-LUNG CHEN |
| 臺大學術典藏 |
2019-08-27T04:12:41Z |
Translational control in the germ plasm: nos-2 RNA regulation
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Pei-Lung Chen; PEI-LUNG CHEN |
| 臺大學術典藏 |
2019-08-27T04:11:26Z |
Tuberous sclerosis complex diagnostic criteria update: recommendations of the 2012 International Tuberous Sclerosis Complex Consensus Conference
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Pei-Lung Chen; PEI-LUNG CHEN |
| 臺大學術典藏 |
2019-08-27T04:10:47Z |
Tuberous sclerosis complex surveillance and management: recommendations of the 2012 International Tuberous Sclerosis Complex Consensus Conference
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Pei-Lung Chen; PEI-LUNG CHEN |
| 臺大學術典藏 |
2019-08-27T03:30:42Z |
Neuregulin 3 Knockout Mice Exhibit Behaviors Consistent with Psychotic Disorders
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Hayes, Lindsay N;Shevelkin, Alexey;Zeledon, Mariela;Steel, Gary;Pei-Lung Chen;Obie, Cassandra;Pulver, Ann;Avramopoulos, Dimitrios;Valle, David;Sawa, Akira;Pletnikov, Mikhail V; Hayes, Lindsay N; Shevelkin, Alexey; Zeledon, Mariela; Steel, Gary; PEI-LUNG CHEN; Obie, Cassandra; Pulver, Ann; Avramopoulos, Dimitrios; Valle, David; Sawa, Akira; Pletnikov, Mikhail V |
| 臺大學術典藏 |
2019-08-27T03:21:13Z |
Plectin Mutations in Progressive Familial Intrahepatic Cholestasis
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HUEY-LING CHEN;PEI-LUNG CHEN;MEI-HWEI CHANG;YUNG-MING JENG;MING-CHIH HO;Liou, Bang-Yu;YEN-HSUAN NI;JIA-FENG WU;Chien, Mu-Ming;Hui-Ling Chen;Hsu, Jacob Shujui;Wu, Shang-Hsin; Wu, Shang-Hsin; Hsu, Jacob Shujui; Hui-Ling Chen; Chien, Mu-Ming; JIA-FENG WU; YEN-HSUAN NI; Liou, Bang-Yu; MING-CHIH HO; YUNG-MING JENG; MEI-HWEI CHANG; PEI-LUNG CHEN; HUEY-LING CHEN |
| 臺大學術典藏 |
2019-08-21T15:23:01Z |
Fine Mapping on Chromosome 10q22-q23 Implicates Neuregulin 3 in Schizophrenia
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PEI-LUNG CHEN; Avramopoulos, Dimitrios; Lasseter, Virginia K.; McGrath, John A.; Fallin, M. Daniele; Liang, Kung Yee; Nestadt, Gerald; Feng, Ningping; Steel, Gary; Cutting, Andrew S.; Wolyniec, Paula; Pulver, Ann E.; Valle, David; Pei-Lung Chen;Avramopoulos, Dimitrios;Lasseter, Virginia K.;Mcgrath, John A.;Fallin, M. Daniele;Liang, Kung Yee;Nestadt, Gerald;Feng, Ningping;Steel, Gary;Cutting, Andrew S.;Wolyniec, Paula;Pulver, Ann E.;Valle, David |
| 臺大學術典藏 |
2019-04-26T07:13:17Z |
P53 ICE CRIM mouse: a tool to generate mutant allelic series in somatic cells and germ lines for cancer studies
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Fan, Hsiang-Hsuan;Yu, I-Shing;Lin, Yin-Hung;Wang, Shin-Yu;Liaw, Ying-Hsuan;Pei-Lung Chen;Tsung-Lin Yang;Shu-Wha Lin;You-Tzung Chen; Fan, Hsiang-Hsuan; Yu, I-Shing; Lin, Yin-Hung; Wang, Shin-Yu; Liaw, Ying-Hsuan; PEI-LUNG CHEN; TSUNG-LIN YANG; SHU-WHA LIN; You-Tzung Chen |
| 臺大學術典藏 |
2019-04-26T06:57:34Z |
Serum levels of insulin-like growth factor 1 are negatively associated with log transformation of thyroid-stimulating hormone in Graves' disease patients with hyperthyroidism or subjects with euthyroidism: A prospective observational study
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Fen-Yu Tseng;Chen, Yen-Ting;Chi, Yu-Chiao;Pei-Lung Chen;Wei-Shiung Yang; FEN-YU TSENG; Chen, Yen-Ting; Chi, Yu-Chiao; PEI-LUNG CHEN; WEI-SHIUNG YANG |
| 臺大學術典藏 |
2019-04-26T06:43:07Z |
A clinical and genetic study of early-onset and familial parkinsonism in taiwan: An integrated approach combining gene dosage analysis and next-generation sequencing
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Chin-Hsien Lin;Pei-Lung Chen;Chun-Hwei Tai;Lin, Hang-I;Chen, Chih-Shan;Chen, Meng-Ling;Ruey-Meei Wu; CHIN-HSIEN LIN; PEI-LUNG CHEN; CHUN-HWEI TAI; Lin, Hang-I; Chen, Chih-Shan; Chen, Meng-Ling; RUEY-MEEI WU |
| 臺大學術典藏 |
2019-04-26T03:48:25Z |
The Lupus-Associated Fcγ Receptor IIb-I232T Polymorphism Results in Impairment in the Negative Selection of Low-Affinity Germinal Center B Cells Via c-Abl in Mice
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SHIANG-JONG TZENG;PEI-LUNG CHEN;Chen, Chih-Shan;Hwai, Haw;Yu, I-Shing;Jhou, Jyun-Pei; Jhou, Jyun-Pei; Yu, I-Shing; Hwai, Haw; Chen, Chih-Shan; PEI-LUNG CHEN; SHIANG-JONG TZENG |
| 臺大學術典藏 |
2019-04-25T08:20:01Z |
Using Ion Torrent sequencing to study genetic mutation profiles of fatal thyroid cancers
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Lin, Chia-Chi;Cheng, Wern-Cherng;PEI-LUNG CHEN;KUAN-TING KUO;Chang, Ching-Chung;KUEN-YUAN CHEN;Lu, Jin-Ying; Lu, Jin-Ying; Cheng, Wern-Cherng; KUEN-YUAN CHEN; Lin, Chia-Chi; Chang, Ching-Chung; KUAN-TING KUO; PEI-LUNG CHEN |
| 臺大學術典藏 |
2019-04-25T08:08:46Z |
A 1204-single nucleotide polymorphism and insertion-deletion polymorphism panel for massively parallel sequencing analysis of DNA mixtures
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Yin, Hsiang-I;Li, Huei-Ying;Chung, Wan-Chia;JAMES CHUN-I LEE;CHIH-PENG LIN;PEI-LUNG CHEN;HSIAO-LIN HWA; HSIAO-LIN HWA; Chung, Wan-Chia; PEI-LUNG CHEN; CHIH-PENG LIN; Li, Huei-Ying; Yin, Hsiang-I; JAMES CHUN-I LEE |
| 臺大學術典藏 |
2019-04-25T07:09:27Z |
Early measurement of IL-10 predicts the outcomes of patients with acute respiratory distress syndrome receiving extracorporeal membrane oxygenation
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Liu, Tze-Tze;Lai, Chien-Heng;Wu, Shu-Wei;Tsai, Pi-Ru;Ko, Wen-Je;Liu, Chia-Hsiung;TZUU-SHUH JOU;SHU-CHIEN HUANG;PEI-LUNG CHEN;YIH-SHARNG CHEN;CHIH-HSIEN WANG;SHUENN-WEN KUO; Liu, Chia-Hsiung; SHUENN-WEN KUO; Ko, Wen-Je; Tsai, Pi-Ru; Wu, Shu-Wei; Lai, Chien-Heng; CHIH-HSIEN WANG; YIH-SHARNG CHEN; PEI-LUNG CHEN; Liu, Tze-Tze; SHU-CHIEN HUANG; TZUU-SHUH JOU |
| 臺大學術典藏 |
2019-04-25T07:07:11Z |
Identification of VPS35 p.D620N mutation-related Parkinson's disease in a Taiwanese family with successful bilateral subthalamic nucleus deep brain stimulation: a case report and literature review
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Lan, Min-Yu;Chang, Yung-Yee;Chen, Ying-Fa;CHIN-HSIEN LIN;PEI-LUNG CHEN; Chen, Ying-Fa; Chang, Yung-Yee; Lan, Min-Yu; PEI-LUNG CHEN; CHIN-HSIEN LIN |
| 臺大學術典藏 |
2019-04-25T06:54:26Z |
Intrafamilial phenotypic heterogeneity in a Taiwanese family with a MAPT p.R5H mutation: a case report and literature review
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Chen, Pei-Hao;Lin, Hui-Chi;SHIH-JUNG CHENG;PEI-LUNG CHEN;CHIN-HSIEN LIN; Lin, Hui-Chi; CHIN-HSIEN LIN; PEI-LUNG CHEN; SHIH-JUNG CHENG; Chen, Pei-Hao |
| 臺大學術典藏 |
2019-04-25T06:34:26Z |
KCNN2 polymorphisms and cardiac tachyarrhythmias
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Lin, Lian-Yu;Chen, Chi-Ling;Wu, Cho-Kai;JIUNN-LEE LIN;WEI-SHIUNG YANG;LING-PING LAI;Ho, Li-Ting;JYH-MING JIMMY JUANG;Chen, Peng-Sheng;FU-TIEN CHIANG;Chiu, Fu-Chun;PEI-LUNG CHEN;CHIA-TI TSAI;CHIH-CHIEH YU; CHIH-CHIEH YU; CHIA-TI TSAI; PEI-LUNG CHEN; Wu, Cho-Kai; Chiu, Fu-Chun; FU-TIEN CHIANG; Chen, Peng-Sheng; Chen, Chi-Ling; Lin, Lian-Yu; JYH-MING JIMMY JUANG; Ho, Li-Ting; LING-PING LAI; WEI-SHIUNG YANG; JIUNN-LEE LIN |
| 臺大學術典藏 |
2019-04-24T08:03:41Z |
Follicular thyroid carcinoma with NRAS Q61K and GNAS R201H mutations that had a good (131)I treatment response
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Lu, Jin-Ying;Hung, Po-Ju;Pei-Lung Chen;Ruoh-Fang Yen;Kuan-Ting Kuo;Tsung-Lin Yang;Chih-Yuan Wang;Tien-Chun Chang;Tien-Shang Huang;Chang, Ching-Chung; Lu, Jin-Ying; Hung, Po-Ju; PEI-LUNG CHEN; RUOH-FANG YEN; KUAN-TING KUO; TSUNG-LIN YANG; CHIH-YUAN WANG; TIEN-CHUN CHANG; TIEN-SHANG HUANG; Chang, Ching-Chung |
| 臺大學術典藏 |
2019-03-04T07:58:39Z |
Oncogenic Function of a KIF5B-MET Fusion Variant in Non-Small Cell Lung Cancer
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Tsai, Meng Feng;Tsai, Tzu Hsiu;Luo, Sheng Ching;Chang, Shih Han;Li, Huei Ying;Liu, Yi-Nan;Gow, Chien Hung;JIN-YUAN SHIH;PEI-LUNG CHEN;MIN-SHU HSIEH; Gow, Chien Hung; Liu, Yi-Nan; Li, Huei Ying; MIN-SHU HSIEH; Chang, Shih Han; Luo, Sheng Ching; Tsai, Tzu Hsiu; PEI-LUNG CHEN; Tsai, Meng Feng; JIN-YUAN SHIH |
| 臺大學術典藏 |
2018-09-10T15:27:55Z |
Genetic determinants of antithyroid drug-induced agranulocytosis by human leukocyte antigen genotyping and genome-wide association study
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Chu, Chen-Chung; Chu, Chen-Chung; WEI-SHIUNG YANG; Lin, Jung-Hsin; Lin, Jung-Hsin; Chen, Szu-Chi; PEI-LUNG CHEN; Chen, Szu-Chi; Chen, Szu-Chi; Chang, Ching-Chung; TIEN-SHANG HUANG; Chang, Ching-Chung; Huang, Tien-Shang; Tsai, Keh Sung; Tsai, Keh Sung; Tsai, Keh Sung; Tseng, Fen-Yu; Tseng, Fen-Yu; Tseng, Fen-Yu; Wang, Chih-Yuan; Wang, Chih-Yuan; Wang, Chih-Yuan; Lu, Jin-Ying; Lu, Jin-Ying; Lu, Jin-Ying; Chiu, Wei-Yih; Chiu, Wei-Yih; Chiu, Wei-Yih; Chang, Chien-Ching; Chen, Yu-Hsuan; Chen, Yu-Hsuan; Chen, Yuan-Tsong; Chen, Yuan-Tsong; Fann, Cathy Shen-Jang; Fann, Cathy Shen-Jang; Yang, Wei-Shiung; Yang, Wei-Shiung; Chang, Tien-Chun; Chang, Tien-Chun; Chang, Tien-Chun; 顏娟英; Chen, Pei-Lung;Shih, Shyang-Rong;Wang, Pei-Wen;Lin, Ying-Chao;Chu, Chen-Chung;Lin, Jung-Hsin;Chen, Szu-Chi;Chang, Ching-Chung;Huang, Tien-Shang;Tsai, Keh Sung;Tseng, Fen-Yu;Wang, Chih-Yuan;Lu, Jin-Ying;Chiu, Wei-Yih;Chang, Chien-Ching;Chen, Yu-Hsuan;Chen, Yuan-Tsong;Fann, Cathy Shen-Jang;Yang, Wei-Shiung;Chang, Tien-Chun; 蔡克嵩;陳燕惠;黃天祥;張慶忠;林榮信;曾芬郁;呂金盈;楊偉勛;張天鈞;王治元;邱偉益;陳沛隆;施翔蓉; 蔡克嵩;陳燕惠;黃天祥;張慶忠;林榮信;曾芬郁;呂金盈;楊偉勛;張天鈞;王治元;邱偉益;陳沛隆;施翔蓉; 蔡克嵩;陳燕惠;黃天祥;張慶忠;林榮信;曾芬郁;呂金盈;楊偉勛;張天鈞;王治元;邱偉益;陳沛隆;施翔蓉; SHYANG-RONG SHIH; Chen, Pei-Lung; Chen, Pei-Lung; Chen, Pei-Lung; WEI-YIH CHIU; Shih, Shyang-Rong; Shih, Shyang-Rong; Shih, Shyang-Rong; Wang, Pei-Wen; Wang, Pei-Wen; KEH-SUNG TSAI; Wang, Pei-Wen; TIEN-CHUN CHANG; Lin, Ying-Chao; Lin, Ying-Chao; FEN-YU TSENG; Chen, P.-L. and Shih, S.-R. and Wang, P.-W. and Lin, Y.-C. and Chu, C.-C. and Lin, J.-H. and Chen, S.-C. and Chang, C.-C. and Huang, T.-S. and Tsai, K.S. and Tseng, F.-Y. and Wang, C.-Y. and Lu, J.-Y. and Chiu, W.-Y. and Chang, C.-C. and Chen, Y.-H. and Chen, Y.-T. and Fann, C.S.-J. and Yang, W.-S. and Chang, T.-C. |
| 臺大學術典藏 |
2018-09-10T15:17:42Z |
Concurrent exome-targeted next-generation sequencing and single nucleotide polymorphism array to identify the causative genetic aberrations of isolated Mayer-Rokitansky-Küster-Hauser syndrome
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PEI-LUNG CHEN; Li, Huei-Ying; Ho, Hong-Nerng; Yang, Yu-Shih; Chen, Pei-Lung; Chen, M.-J. and Wei, S.-Y. and Yang, W.-S. and Wu, T.-T. and Li, H.-Y. and Ho, H.-N. and Yang, Y.-S. and Chen, P.-L.; 周妍君; Chen, Mei-Jou;Wei, Shin-Yi;Yang, Wei-Shiung;Wu, Tsai-Tzu;Li, Huei-Ying;Ho, Hong-Nerng;Yang, Yu-Shih;Chen, Pei-Lung; 楊友仕;陳美州;楊偉勛;何弘能;陳沛隆; 楊友仕;陳美州;楊偉勛;何弘能;陳沛隆; Chou, Yen-Chun; YU-SHIH YANG; Chen, Mei-Jou; Chou, Yen-Chun; HONG-NERNG HO; Wei, Shin-Yi; MEI-JOU CHEN; Yang, Wei-Shiung; Wu, Tsai-Tzu; WEI-SHIUNG YANG |
| 臺大學術典藏 |
2018-09-10T14:50:37Z |
Genetic Analysis of CARD14 in Non-familial Pityriasis Rubra Pilaris: A Case Series.
|
TSEN-FANG TSAI;Tsai, Tsen-Fang;PEI-LUNG CHEN;Chen, You-Tzung;Jin-Bon Hong;Chen, Pei-Lung;Hong, Jin-Bon;You-Tzung Chen; You-Tzung Chen; Hong, Jin-Bon; JIN-BON HONG; PEI-LUNG CHEN; Tsai, Tsen-Fang |
| 臺大學術典藏 |
2018-09-10T09:42:02Z |
Tuberous sclerosis complex surveillance and management: recommendations of the 2012 International Tuberous Sclerosis Complex Consensus Conference.
|
PEI-LUNG CHEN; Pei-Lung Chen |
| 臺大學術典藏 |
2018-09-10T09:42:02Z |
Tuberous sclerosis complex diagnostic criteria update: recommendations of the 2012 Iinternational Tuberous Sclerosis Complex Consensus Conference.
|
Pei-Lung Chen; PEI-LUNG CHEN |
| 臺大學術典藏 |
2018-09-10T09:38:42Z |
Gene-wide tagging study of the effects of common genetic polymorphisms in the α subunits of the GABAA receptor on epilepsy treatment response
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Hung, C.-C.;Chen, P.-L.;Huang, W.-M.;Tai, J.J.;Hsieh, T.-J.;Ding, S.-T.;Hsieh, Y.-W.;Liou, H.-H.; Hung, C.-C.; Chen, P.-L.; Huang, W.-M.; Tai, J.J.; Hsieh, T.-J.; Ding, S.-T.; Hsieh, Y.-W.; Liou, H.-H.; SHIH-TORNG DING; PEI-LUNG CHEN |
| 臺大學術典藏 |
2018-09-10T09:38:42Z |
Identification of a novel HLA-B allele, B*07:162, in a Taiwanese individual
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Chen, P.-L.;Lai, S.-K.;Yang, W.-S.;Chang, T.-C.;Chu, C.-C.; TIEN-CHUN CHANG; WEI-SHIUNG YANG; PEI-LUNG CHEN |
| 臺大學術典藏 |
2018-09-10T09:12:57Z |
An isodicentric X chromosome with gonadal dysgenesis in a lady without prominent somatic features of Turner's syndrome. A case report
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Yu, T.-Y.;Lin, H.-S.;Chen, P.-L.;Huang, T.-S.; PEI-LUNG CHEN; TIEN-SHANG HUANG |
| 臺大學術典藏 |
2018-09-10T09:12:57Z |
Common genetic mutations in the start codon of the SDH subunit D gene among Chinese families with familial head and neck paragangliomas
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Wang, C.-P. and Chen, T.-C. and Chang, Y.-L. and Ko, J.-Y. and Yang, T.-L. and Lo, F.-Y. and Hu, Y.-L. and Chen, P.-L. and Wu, C.-C. and Lou, P.-J.; YIH-LEONG CHANG; TSUNG-LIN YANG; CHENG-PING WANG; PEI-LUNG CHEN; CHEN-CHI WU; PEI-JEN LOU |
| 臺大學術典藏 |
2018-09-10T08:28:22Z |
Comprehensive genotyping in two homogeneous Graves' disease samples reveals major and novel HLA association alleles
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Chen, P.-L.; Fann, C.-S.-J.; Chu, C.-C.; Chang, C.-C.; Chang, S.-W.; Hsieh, H.-Y.; Lin, M.; Yang, W.-S.; Chang, T.-C.; TIEN-CHUN CHANG; WEI-SHIUNG YANG; PEI-LUNG CHEN; CHEN, PEI-LUNG; FANN, CATHY SHENG-JIUAN; CHU, CHEN- CHUNG; CHANG, CHIEN-CHING; CHANG, SU-WEI; HSIEH, HSIN-YI; LIN, CHU-MARIE; YANG, WEI-SHIUNG; CHANG, TIEN-CHUN |
| 臺大學術典藏 |
2018-09-10T08:28:22Z |
Linkage and association on 8p21.2-p21.1 in schizophrenia
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Fallin, M.D. Lasseter, V.K. Liu, Y. Avramopoulos, D. Mcgrath, J. Wolyniec, P.S. Nestadt, G. Liang, K.-Y. Chen, P.-L. Valle, D. Pulver, A.E.; PEI-LUNG CHEN |
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