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[Analysis of SATB2 gene mutation in a child with Glass syndrome].
Lin M, Yao R, Lu J, Chen W, Xu Y, Li G, Yu T, Qing Y, Jin X, Wang J. Lin M, et al. Among authors: qing y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Jul 10;36(7):712-715. doi: 10.3760/cma.j.issn.1003-9406.2019.07.014. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31302918 Chinese.
Novel pathogenic ACAN variants in non-syndromic short stature patients.
Hu X, Gui B, Su J, Li H, Li N, Yu T, Zhang Q, Xu Y, Li G, Chen Y, Qing Y; Chinese Genetic Short Stature Consortium; Li C, Luo J, Fan X, Ding Y, Li J, Wang J, Wang X, Chen S, Shen Y. Hu X, et al. Among authors: qing y. Clin Chim Acta. 2017 Jun;469:126-129. doi: 10.1016/j.cca.2017.04.004. Epub 2017 Apr 7. Clin Chim Acta. 2017. PMID: 28396070
Increased transactivation and impaired repression of β-catenin-mediated transcription associated with a novel SOX3 missense mutation in an X-linked hypopituitarism pedigree with modest growth failure.
Yu T, Chang G, Cheng Q, Yao R, Li J, Xu Y, Li G, Ding Y, Qing Y, Li N, Shen Y, Wang X, Wang J. Yu T, et al. Among authors: qing y. Mol Cell Endocrinol. 2018 Dec 15;478:133-140. doi: 10.1016/j.mce.2018.08.006. Epub 2018 Aug 17. Mol Cell Endocrinol. 2018. PMID: 30125608