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Transmission of a Novel Imprinting Center Deletion Associated With Prader-Willi Syndrome Through Three Generations of a Chinese Family: Case Presentation, Differential Diagnosis, and a Lesson Worth Thinking About.
Zhang K, Liu S, Gu W, Lv Y, Yu H, Gao M, Wang D, Zhao J, Li X, Gai Z, Zhao S, Liu Y, Yuan Y. Zhang K, et al. Among authors: liu y, liu s. Front Genet. 2021 Aug 24;12:630650. doi: 10.3389/fgene.2021.630650. eCollection 2021. Front Genet. 2021. PMID: 34504512 Free PMC article.
[Analysis of a case with Mowat-Wilson syndrome caused by ZEB2 gene variant].
Ma J, Liu Y, Zhang K, Lyu Y, Gao M, Wang D, Gai Z, Liu Y. Ma J, et al. Among authors: liu y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020 May 10;37(5):539-542. doi: 10.3760/cma.j.issn.1003-9406.2020.05.011. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020. PMID: 32335881 Chinese.
[Clinical and genetic analysis of a patient with rare nephronophthisis].
Wang D, Tong G, Dong R, Lyu Y, Gao M, Ma J, Wan Y, Pang H, Gai Z, Liu Y. Wang D, et al. Among authors: liu y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020 Jul 10;37(7):743-746. doi: 10.3760/cma.j.issn.1003-9406.2020.07.010. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020. PMID: 32619255 Chinese.
208,674 results
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