Ngā hua rapu - Wang, Lin‐Ping
- E whakaatu ana i te 1 - 10 hua o te 10
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Analysis of SLC4A11, ZEB1, LOXHD1, COL8A2 and TCF4 gene sequences in a multi-generational family with late-onset Fuchs corneal dystrophy mā TANG, HUI, ZHANG, WEN, YAN, XIN-MIN, WANG, LIN-PING, DONG, HONG, SHOU, TAO, LEI, HUO, GUO, QIANG
I whakaputaina 2016Text -
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Whole exome sequencing identified a pathogenic nonsense mutation in LMNA in a family with a progressive cardiac conduction defect: A case report mā Fan, Peng, Zhang, Di, Yang, Kun-Qi, Tian, Tao, Luo, Fang, Liu, Ya-Xin, Wang, Lin-Ping, Zhou, Xian-Liang
I whakaputaina 2020Text -
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Forkhead Box Q1 Is Critical to Angiogenesis and Macrophage Recruitment of Colorectal Cancer mā Tang, Hui, Zheng, Ji, Bai, Xuan, Yue, Ke-Lin, Liang, Jian-Hua, Li, Dan-Yang, Wang, Lin-Ping, Wang, Jin-Li, Guo, Qiang
I whakaputaina 2020Text -
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Tuberculosis in Takayasu arteritis: a retrospective study in 1105 Chinese patients mā Zhang, Ying, Fan, Peng, Luo, Fang, Zhang, Hui-Min, Song, Lei, Ma, Wen-Jun, Wu, Hai-Ying, Cai, Jun, Wang, Lin-Ping, Zhou, Xian-Liang
I whakaputaina 2019Text -
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Prevalence of Liddle Syndrome Among Young Hypertension Patients of Undetermined Cause in a Chinese Population mā Wang, Lin‐Ping, Yang, Kun‐Qi, Jiang, Xiong‐Jing, Wu, Hai‐Ying, Zhang, Hui‐Min, Zou, Yu‐Bao, Song, Lei, Bian, Jin, Hui, Ru‐Tai, Liu, Ya‐Xin, Zhou, Xian‐Liang
I whakaputaina 2015Text -
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A novel PRKAG2 mutation in a Chinese family with cardiac hypertrophy and ventricular pre-excitation mā Yang, Kun-Qi, Lu, Chao-Xia, Zhang, Ying, Yang, Yan-Kun, Li, Jia-Cheng, Lan, Tian, Meng, Xu, Fan, Peng, Tian, Tao, Wang, Lin-Ping, Liu, Ya-Xin, Zhang, Xue, Zhou, Xian-Liang
I whakaputaina 2017Text -
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Pediatric Liddle Syndrome Caused by a Novel SCNN1G Variant in a Chinese Family and Characterized by Early-Onset Hypertension mā Fan, Peng, Pan, Xiao-Cheng, Zhang, Di, Yang, Kun-Qi, Zhang, Ying, Tian, Tao, Luo, Fang, Ma, Wen-Jun, Liu, Ya-Xin, Wang, Lin-Ping, Zhang, Hui-Min, Song, Lei, Cai, Jun, Zhou, Xian-Liang
I whakaputaina 2020Text -
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Apparent mineralocorticoid excess caused by novel compound heterozygous mutations in HSD11B2 and characterized by early-onset hypertension and hypokalemia mā Fan, Peng, Lu, Yi-Ting, Yang, Kun-Qi, Zhang, Di, Liu, Xue-Ying, Tian, Tao, Luo, Fang, Wang, Lin-Ping, Ma, Wen-Jun, Liu, Ya-Xin, Zhang, Hui-Min, Song, Lei, Cai, Jun, Lou, Ying, Zhou, Xian-Liang
I whakaputaina 2020Text