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Genetic and Phenotype Analysis of a Chinese Cohort of Infants and Children With Epilepsy.
Chuan Z, Ruikun C, Qian L, Shiyue M, Shengju H, Yong Y, Haibo L, Neng X, Yong Z, Huiqin X, Weijia W, Ling H, Bingbo Z, Zhang Q, Yan W, Zongfu C, Xu M. Chuan Z, et al. Among authors: zhang q. Front Genet. 2022 Apr 27;13:869210. doi: 10.3389/fgene.2022.869210. eCollection 2022. Front Genet. 2022. PMID: 35571021 Free PMC article.
[Genetic analysis of 21 cases of methylmalonic acidemia].
Wang X, Sun X, Hao S, Liu F, Zhang Q, Zheng L, Zhang C. Wang X, et al. Among authors: zhang c, zhang q. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022 Apr 10;39(4):362-365. doi: 10.3760/cma.j.cn511374-20201218-00889. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022. PMID: 35446966 Chinese.
[Genetic analysis and prenatal diagnosis for a Chinese pedigree affected with co-morbid Ornithine carbamoyl transferase deficiency and MECP2 duplication syndrome].
Zhang Q, Hao S, Hui L, Zheng L, Wang X, Feng X, Liu F, Chen X, Zhou B, Wang Y, Zhang C. Zhang Q, et al. Among authors: zhang c. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2024 Mar 10;41(3):306-311. doi: 10.3760/cma.j.cn511374-20221202-00828. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2024. PMID: 38448019 Chinese.
A novel LOXHD1 variant in a Chinese couple with hearing loss.
Zhang C, Hao S, Liu Y, Zhou B, Liu F, Zheng L, Ma P, Liu Q, Lin X, Yan Y, Zhang Q. Zhang C, et al. Among authors: zhang q. J Int Med Res. 2019 Dec;47(12):6082-6090. doi: 10.1177/0300060519884197. Epub 2019 Nov 10. J Int Med Res. 2019. PMID: 31709873 Free PMC article.
64,126 results
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