Showing 1 - 8 results of 8 for search 'Ruolan Guo', query time: 0.32s
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Identification of novel homozygous nonsense SLC10A7 variant causing short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis and surgical management of spine by Wenyan Zhang, Ziming Yao, Ruolan Guo, Jun Cao, Wei Li, Chanjuan Hao, Xuejun Zhang
Published 2023-11-01
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Phenylalanyl-tRNA synthetase deficiency caused by biallelic variants in FARSA gene and literature review by Ruolan Guo, Yuanying Chen, Xuyun Hu, Zhan Qi, Jun Guo, Yuchuan Li, Chanjuan Hao
Published 2023-10-01
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Identification of a novel variant in N-cadherin associated with dilated cardiomyopathy by Yuanying Chen, Yuanying Chen, Qiqing Sun, Chanjuan Hao, Chanjuan Hao, Ruolan Guo, Ruolan Guo, Chentong Wang, Chentong Wang, Weili Yang, Yaodong Zhang, Fangjie Wang, Wei Li, Wei Li, Jun Guo, Jun Guo
Published 2022-08-01
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CASQ2 variants in Chinese children with catecholaminergic polymorphic ventricular tachycardia by Qirui Li, Ruolan Guo, Lu Gao, Lang Cui, Zhihui Zhao, Xia Yu, Yue Yuan, Xiwei Xu
Published 2019-11-01
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Case report: Clinical features and prognosis of two Infants with rhabdomyosarcoma of the tongue by Peiyi Yang, Na Xu, Yan Su, Chao Duan, Shengcai Wang, Libing Fu, Tong Yu, Ruolan Guo, Xiaoli Ma
Published 2023-01-01
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Behavioural deficits of autism spectrum disorder and associations with different gene clusters: a study with the whole-genome transmission disequilibrium test by Wei Li, Qi Guo, Peng Zhang, Yue Zhang, Kun Xia, Lu Xia, Xin Ni, Ruolan Guo, Wenjian Xu, Chunlin Zhao, Ting Bai, Chanjuan Hao
Published 2023-12-01
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