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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. Among authors: wang y. 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: wang g, wang 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: wang j, wang 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.
[Molecular genetic analysis of a child with de novo 16p11.2 microdeletion].
Zhuang J, Wang Y, Zeng S, Wang J, Jiang Y. Zhuang J, et al. Among authors: wang j, wang y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020 Nov 10;37(11):1283-1286. doi: 10.3760/cma.j.cn511374-20190805-00397. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020. PMID: 33179241 Chinese.
297,646 results
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