Human Genome Epidemiology Literature Finder
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Records 1 - 5 (of 5 Records) |
| Query Trace: Disease and ITGB4[original query] |
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| A Systematic Analysis of Major Susceptible Genes in Childhood-onset Steroid-resistant Nephrotic Syndrome. Annals of clinical and laboratory science 2019 7 49 (3): 330-337. Li Yongzhen, He Qingnan, Wang Ying, Dang Xiqiang, Wu Xiaochuan, Li Xiaoyan, Shuai Lanjun, Yi Zhuw |
| Common variants of NRG1 and ITGB4 confer risk of Hirschsprung disease in Han Chinese population. Journal of pediatric surgery 2020 Apr . Wei Zhiliang, Yu Xianxian, Wu Wenjie, Bai Meirong, Lu Yanjiao, Song Huanlei, Gong Yiming, Gu Beilin, Chu Xun, Cai W |
| Whole Exome Sequencing Identifies Two Novel Mutations in a Patient with UC Associated with PSC and SSA. Canadian journal of gastroenterology & hepatology 2021 9 2021 9936932. Wu Dong, Chen Dan, Shi Wen, Liu Wei, Zhou Weixun, Qian Jiami |
| Whole-Exome Sequencing Reveals Rare Germline Mutations in Patients With Hemifacial Microsomia. Frontiers in genetics 2021 6 12 580761. Chen Xiaojun, Liu Fatao, Mar Aung Zin, Zhang Yan, Chai Ga |
| Idiopathic collapsing glomerulopathy is associated with APOL1 high-risk genotypes or Mendelian variants in most affected individuals in a highly admixed population. Kidney international 2023 12 . Precil D Neves, Andreia Watanabe, Elieser H Watanabe, Amanda M Narcizo, Kelly Nunes, Antonio M Lerario, Frederico Moraes Ferreira, Lívia B Cavalcante, Janewit Wongboonsin, Denise M Malheiros, Lectícia B Jorge, Matthew G Sampsom, Irene L Noronha, Luiz F Onuch |
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