Search Results - Weiyue Gu
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1
Correction to: Digenic inheritance of SLC12A3 and CLCNKB genes in a Chinese girl with Gitelman syndrome by Yuanmei Kong, Ke Xu, Ke Yuan, Jianfang Zhu, Weiyue Gu, Li Liang, Chunlin Wang
Published 2019Call Number: Loading…Connect to this object online.
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2
The first case of intellectual disability caused by novel compound heterozygosity for NUDT2 variants by Bo Bi, Xiaohong Chen, Shan Huang, Min Peng, Weiyue Gu, Hongmin Zhu, Yangcan Ming
Published 2024Call Number: Loading…Connect to this object online.
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3
Case Report: Novel CA12 Homozygous Variant Causing Isolated Hyperchloridrosis in a Chinese Child With Hyponatremia by Meigui Han, Min Peng, Ziming Han, Xiaojuan Zhu, Qian Huang, Weiyue Gu, Yong Guo
Published 2022Call Number: Loading…Connect to this object online.
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4
Digenetic inheritance of SLC12A3 and CLCNKB genes in a Chinese girl with Gitelman syndrome by Yuanmei Kong, Ke Xu, Ke Yuan, Jianfang Zhu, Weiyue Gu, Li Liang, Chunlin Wang
Published 2019Call Number: Loading…Connect to this object online.
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5
A comprehensive multiplex PCR based exome-sequencing assay for rapid bloodspot confirmation of inborn errors of metabolism by Wenjie Wang, Jianping Yang, Jinjie Xue, Wenjuan Mu, Xiaogang Zhang, Wang Wu, Mengnan Xu, Yuyan Gong, Yiqian Liu, Yu Zhang, Xiaobing Xie, Weiyue Gu, Jigeng Bai, David S. Cram
Published 2019Call Number: Loading…Connect to this object online.
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