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[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: feng x. 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.
162 results