臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)

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Institution	Date	Title	Author
國立成功大學	2023-11-30	Associations between maternal chronic diseases and congenital anomalies of the kidney and urinary tract in offspring: a population-based cohort study	Chou;Hsin-Hsu;Chen;Chih-Chia;Tsai;Ching-Fang;Kuo;Pao-Lin;Chiou;Yuan-Yow
國立成功大學	2023-06	Preterm birth and weight-for-gestational age for risks of autism spectrum disorder and intellectual disability: A nationwide population-based cohort study	Chang;-Shan, Yu;Chen;-Wen, Li;Yu;Tsung;Lin;Sheng-Hsiang;Kuo;Pao-Lin
國立成功大學	2023-03	Proper phosphorylation of septin 12 regulates septin 4 and soluble adenylyl cyclase expression to induce sperm capacitation	Wang;Han-Yu;Shen;Yi-Ru;Tsai;Yung-Chieh;Wu;Shang-Rung;Wang;Chia-Yih;Kuo;Pao-Lin
國立成功大學	2022-09-5	Increased risk of early-onset childhood systemic lupus erythematosus for children born to affected parents: A nationwide child-parent cohort study	Wu;Chun-Hsin;Chen;Chih-An;Lin;Sheng-Hsiang;Weng;Chia-Tse;Kuo;Pao-Lin;Shieh;Chi-Chang
國立成功大學	2022-09	Novel mutation of MAP3K1 gene in 46,XY DSD with complete gonadal dysgenesis	Yu;Pei-Hsiu;Tsai;Meng-Che;Chiang;-Ting, Chun;Wang;Han-Yu;Kuo;Pao-Lin
國立成功大學	2022-07	Incontinentia pigmenti in a male infant and a proposed diagnostic algorithm	Yang;Min-Chia;Lin;Yu-Chen;Huang;Chien-Hao;Ko;Tsang-Ming;Tsai;Meng-Che;Kuo;Pao-Lin;Lee;Julia, Yu-Yun;McGrath;John, A.;Hsu;Chao-Kai
國立成功大學	2022-05	Whole exome sequencing identifies a novel FRAS1 mutation and aids in vitro fertilization with preimplantation genetic diagnosis in Fraser syndrome	Ou;Tsung-Ying;Tsai;Meng-Che;Kuo;Pao-Lin;Lee;Ni-Chung;Chou;Yen-Yin
國立成功大學	2022-04-29	Effects of Septin-14 Gene Deletion on Adult Cognitive/Emotional Behavior	Chen;Kuan-Ru;Wang;Han-Yu;Liao;Yi-Han;Sun;Li-Han;Huang;Yu-Han;Yu;Lung;Kuo;Pao-Lin
國立成功大學	2022-01	Recurrent Fetal Anophthalmia Caused by retinoids acid gene 6 mutations: Correlation between prenatal ultrasonography, magnetic resonance imaging, and pathology	Chiang;Chia-Jung;Cheng;Yueh-Chin;Tsai;Yi-Shan;Kuo;Pao-Lin;Chang;Chiung-Hsin
國立成功大學	2022-01	Complex rearrangements of Y chromosome suggest RPS4Y1 as lymphedema candidate gene	Chen;Po-Fan;Kuan;Long-Ching;Kao;Chiu-Ching;Hsu;Hui-Kuo;Chen;Ming;Kuo;Tsung-Cheng;Kuo;Pao-Lin

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