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Table representation of search results timeline featuring number of search results per year.

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2007 3
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54 results

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Page 1
BMPR1B mutation causes Pierre Robin sequence.
Yang Y, Yuan J, Yao X, Zhang R, Yang H, Zhao R, Guo J, Jin K, Mei H, Luo Y, Zhao L, Tu M, Zhu Y. Yang Y, et al. Among authors: tu m. Oncotarget. 2017 Apr 18;8(16):25864-25871. doi: 10.18632/oncotarget.16531. Oncotarget. 2017. PMID: 28418932 Free PMC article.
SNAI2 mutation causes human piebaldism.
Yang YJ, Zhao R, He XY, Li LP, Chen W, Wang KW, Zhao L, Tu M, Tang JS, Xie ZG, Zhu YM. Yang YJ, et al. Among authors: tu m. Am J Med Genet A. 2014 Mar;164A(3):855-7. doi: 10.1002/ajmg.a.36332. Epub 2014 Jan 17. Am J Med Genet A. 2014. PMID: 24443330 No abstract available.
SMAD6 is frequently mutated in nonsyndromic radioulnar synostosis.
Yang Y, Zheng Y, Li W, Li L, Tu M, Zhao L, Mei H, Zhu G, Zhu Y. Yang Y, et al. Among authors: tu m. Genet Med. 2019 Nov;21(11):2577-2585. doi: 10.1038/s41436-019-0552-8. Epub 2019 May 29. Genet Med. 2019. PMID: 31138930 Free article.
54 results