Search Results - Yixi Sun
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Case Report: Prenatal Diagnosis for a Rett Syndrome Family Caused by a Novel MECP2 Deletion With Heteroduplexes of PCR Product by Honghong Zhang, Yixi Sun, Yixi Sun, Yuxia Zhu, Jiali Hong, Miaomiao Zheng
Published 2021Call Number: Loading…Connect to this object online.
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2
Corrigendum: Case Report: Prenatal Diagnosis for a Rett Syndrome Family Caused by a Novel MECP2 Deletion With Heteroduplexes of PCR Product by Honghong Zhang, Yixi Sun, Yixi Sun, Yuxia Zhu, Jiali Hong, Miaomiao Zheng
Published 2022Call Number: Loading…Connect to this object online.
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3
Novel homozygous silent mutation of ITGB3 gene caused Glanzmann thrombasthenia by Zhengrong Wang, Zhengrong Wang, Yuqing Xu, Yuqing Xu, Yixi Sun, Yixi Sun, Shuang Wang, Shuang Wang, Minyue Dong, Minyue Dong
Published 2023Call Number: Loading…Connect to this object online.
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4
Case report: A compound heterozygous mutations in ASNS broadens the spectrum of asparagine synthetase deficiency in the prenatal diagnosis by Linyan Zhu, Linyan Zhu, Yixi Sun, Yixi Sun, Yuqing Xu, Yuqing Xu, Pengzhen Jin, Pengzhen Jin, Huiqing Ding, Minyue Dong, Minyue Dong
Published 2023Call Number: Loading…Connect to this object online.
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