Canlyniadau Chwilio - Yixi Sun

Case Report: Prenatal Diagnosis for a Rett Syndrome Family Caused by a Novel MECP2 Deletion With Heteroduplexes of PCR Product gan Honghong Zhang, Yixi Sun, Yixi Sun, Yuxia Zhu, Jiali Hong, Miaomiao Zheng

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Corrigendum: Case Report: Prenatal Diagnosis for a Rett Syndrome Family Caused by a Novel MECP2 Deletion With Heteroduplexes of PCR Product gan Honghong Zhang, Yixi Sun, Yixi Sun, Yuxia Zhu, Jiali Hong, Miaomiao Zheng

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Novel homozygous silent mutation of ITGB3 gene caused Glanzmann thrombasthenia gan Zhengrong Wang, Zhengrong Wang, Yuqing Xu, Yuqing Xu, Yixi Sun, Yixi Sun, Shuang Wang, Shuang Wang, Minyue Dong, Minyue Dong

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Case report: A compound heterozygous mutations in ASNS broadens the spectrum of asparagine synthetase deficiency in the prenatal diagnosis gan Linyan Zhu, Linyan Zhu, Yixi Sun, Yixi Sun, Yuqing Xu, Yuqing Xu, Pengzhen Jin, Pengzhen Jin, Huiqing Ding, Minyue Dong, Minyue Dong

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