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Showing results for yuan yong yi
Your search for Yun-Myong Yi retrieved no results
A novel variant in FOXC1 associated with atypical Axenfeld-Rieger syndrome.
Wang R, Wang WQ, Li XQ, Zhao J, Yang K, Feng Y, Guo MM, Liu M, Liu X, Wang X, Yuan YY, Gao X, Xu JC. Wang R, et al. Among authors: yuan yy. BMC Med Genomics. 2021 Nov 22;14(1):277. doi: 10.1186/s12920-021-01130-7. BMC Med Genomics. 2021. PMID: 34809627 Free PMC article.
Addition of an affected family member to a previously ascertained autosomal recessive nonsyndromic hearing loss pedigree and systematic phenotype-genotype analysis of splice-site variants in MYO15A.
Yang JY, Wang WQ, Han MY, Huang SS, Wang GJ, Su Y, Xu JC, Fu Y, Kang DY, Yang K, Zhang X, Liu X, Gao X, Yuan YY, Dai P. Yang JY, et al. Among authors: yuan yy. BMC Med Genomics. 2022 Nov 18;15(1):241. doi: 10.1186/s12920-022-01368-9. BMC Med Genomics. 2022. PMID: 36401330 Free PMC article.
53 results