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[Analysis a family with partial Xq deletion].
Jiang Y, Zhuang J, Wang Y, Zhuang Q, Zeng S. Jiang Y, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Oct 10;34(5):688-690. doi: 10.3760/cma.j.issn.1003-9406.2017.05.015. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 28981934 Chinese.
Molecular analysis of a large novel deletion causing α+-thalassemia.
Zhuang J, Tian J, Wei J, Zheng Y, Zhuang Q, Wang Y, Xie Q, Zeng S, Wang G, Pan Y, Jiang Y. Zhuang J, et al. Among authors: jiang y. BMC Med Genet. 2019 May 6;20(1):74. doi: 10.1186/s12881-019-0797-8. BMC Med Genet. 2019. PMID: 31060505 Free PMC article.
[Clinical and genetic study of a child with 15q11.2 microduplication].
Zhuang J, Wang Y, Zeng S, Wang J, Jiang Y. Zhuang J, et al. Among authors: jiang y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020 Jan 10;37(1):64-66. doi: 10.3760/cma.j.issn.1003-9406.2020.01.017. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020. PMID: 31922600 Chinese.
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