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Mutations in Hnrnpa1 cause congenital heart defects.
Yu Z, Tang PL, Wang J, Bao S, Shieh JT, Leung AW, Zhang Z, Gao F, Wong SY, Hui AL, Gao Y, Dung N, Zhang ZG, Fan Y, Zhou X, Zhang Y, Wong DS, Sham PC, Azhar A, Kwok PY, Tam PP, Lian Q, Cheah KS, Wang B, Song YQ. Yu Z, et al. Among authors: wang j, wang b. JCI Insight. 2018 Jan 25;3(2):e98555. doi: 10.1172/jci.insight.98555. eCollection 2018 Jan 25. JCI Insight. 2018. PMID: 29367466 Free PMC article.
A rare variant in MLKL confers susceptibility to ApoE ɛ4-negative Alzheimer's disease in Hong Kong Chinese population.
Wang B, Bao S, Zhang Z, Zhou X, Wang J, Fan Y, Zhang Y, Li Y, Chen L, Jia Y, Li J, Li M, Zheng W, Mu N, Wang L, Yu Z, Wong DSM, Zhang Y, Kwan J, Ka-Fung Mak H, Ambalavanan A, Zhou S, Cai W, Zheng J, Huang S, Rouleau GA, Yang W, Rogaeva E, Ma X, St George-Hyslop P, Chu LW, Song YQ. Wang B, et al. Among authors: wang l, wang j. Neurobiol Aging. 2018 Aug;68:160.e1-160.e7. doi: 10.1016/j.neurobiolaging.2018.03.006. Epub 2018 Mar 10. Neurobiol Aging. 2018. PMID: 29656768
MYH7 Rare Variant in a Family With Double-Chambered Left Ventricle.
Wang J, Zhang X, Wang X, Wang C, Wang F, Wang B. Wang J, et al. Among authors: wang x, wang f, wang c, wang b. Circ Cardiovasc Genet. 2017 Dec;10(6):e001729. doi: 10.1161/CIRCGENETICS.117.001729. Circ Cardiovasc Genet. 2017. PMID: 29237678 No abstract available.
Novel mutation in SP2 in a Chinese pedigree with Neural tube defects.
Liu BH, Wang J, Li CM, Qi L, Song YH, Pan H, Li TY, Wang BB. Liu BH, et al. Among authors: wang bb, wang j. CNS Neurosci Ther. 2018 Oct;24(10):978-980. doi: 10.1111/cns.12988. Epub 2018 May 31. CNS Neurosci Ther. 2018. PMID: 29855149 Free PMC article. No abstract available.
TNFRSF21 mutations cause high myopia.
Pan H, Wu S, Wang J, Zhu T, Li T, Wan B, Liu B, Luo Y, Ma X, Sui R, Wang B. Pan H, et al. Among authors: wang j, wang b. J Med Genet. 2019 Oct;56(10):671-677. doi: 10.1136/jmedgenet-2018-105684. Epub 2019 Jun 12. J Med Genet. 2019. PMID: 31189563
218,294 results
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