Výsledky vyhledávání - Wang, Lin-Ping
- Zobrazuji výsledky 1 - 10 z 10
-
1
-
2
-
3
Analysis of SLC4A11, ZEB1, LOXHD1, COL8A2 and TCF4 gene sequences in a multi-generational family with late-onset Fuchs corneal dystrophy Autor TANG, HUI, ZHANG, WEN, YAN, XIN-MIN, WANG, LIN-PING, DONG, HONG, SHOU, TAO, LEI, HUO, GUO, QIANG
Vydáno 2016Text -
4
Whole exome sequencing identified a pathogenic nonsense mutation in LMNA in a family with a progressive cardiac conduction defect: A case report Autor Fan, Peng, Zhang, Di, Yang, Kun-Qi, Tian, Tao, Luo, Fang, Liu, Ya-Xin, Wang, Lin-Ping, Zhou, Xian-Liang
Vydáno 2020Text -
5
-
6
-
7
Prevalence of Liddle Syndrome Among Young Hypertension Patients of Undetermined Cause in a Chinese Population Autor 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
Vydáno 2015Text -
8
A novel PRKAG2 mutation in a Chinese family with cardiac hypertrophy and ventricular pre-excitation Autor 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
Vydáno 2017Text -
9
Pediatric Liddle Syndrome Caused by a Novel SCNN1G Variant in a Chinese Family and Characterized by Early-Onset Hypertension Autor 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
Vydáno 2020Text -
10
Apparent mineralocorticoid excess caused by novel compound heterozygous mutations in HSD11B2 and characterized by early-onset hypertension and hypokalemia Autor 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
Vydáno 2020Text