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2013 1
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2016 10
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2020 2
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Did you mean yunyun fu (7 results)?
Thyroglobulin gene mutations in Chinese patients with congenital hypothyroidism.
Hu X, Chen R, Fu C, Fan X, Wang J, Qian J, Yi S, Li C, Luo J, Su J, Zhang S, Xie B, Zheng H, Lai Y, Chen Y, Li H, Gu X, Chen S, Shen Y. Hu X, et al. Among authors: fu c. Mol Cell Endocrinol. 2016 Mar 5;423:60-6. doi: 10.1016/j.mce.2016.01.007. Epub 2016 Jan 8. Mol Cell Endocrinol. 2016. PMID: 26777470
Mosaic UPD(7q)mat in a patient with silver Russell syndrome.
Su J, Wang J, Fan X, Fu C, Zhang S, Zhang Y, Qin Z, Li H, Luo J, Li C, Jiang T, Shen Y. Su J, et al. Among authors: fu c. Mol Cytogenet. 2017 Oct 17;10:36. doi: 10.1186/s13039-017-0337-1. eCollection 2017. Mol Cytogenet. 2017. PMID: 29075327 Free PMC article.
de novo interstitial deletions at the 11q23.3-q24.2 region.
Su J, Chen R, Luo J, Fan X, Fu C, Wang J, He S, Hu X, Zhang S, Yi S, Chen S, Shen Y. Su J, et al. Among authors: fu c. Mol Cytogenet. 2016 May 5;9:39. doi: 10.1186/s13039-016-0247-7. eCollection 2016. Mol Cytogenet. 2016. PMID: 27158264 Free PMC article.
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