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Springer Nature6
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✓Human Genetics6
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Li-Fei Yu results 6 · Newest (Page 1/1, per page 25)
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Journal: Human Genetics ×Author: Li-Fei Yu ×Clear All Filters
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Genetic burden and multidimensional predictors in prenatal diagnosis of fetal congenital diaphragmatic herniaNARA Subscribed
Human Genetics · 2025 · Vol. 144 · Issue 9-10 · Springer
Ruibin Huang; Fang Fu; Shanshan Mei; Liyuan Liu; Wei Zhong; Jin Han; Qiuxia Yu; Hang Zhou; Chunling Ma; Li Zhen; Min Pan; Qiong Deng; Jianqin Lu; Xinyi Zhao; Na Zhang; Fei Guo; Huanyi Chen; Xinyue Tan; Fucheng Li; Dongzhi Li; Ru Li; Can Liao
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TMEM151A variants associated with paroxysmal kinesigenic dyskinesiaNARA Subscribed
Human Genetics · 2023 · Vol. 142 · Issue 8 · Springer
Hua lin Huang; Qing xia Zhang; Fei Huang; Xiao yan Long; Zhi Song; Bo Xiao; Guo liang Li; Cai yu Ma; Ding Liu
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Prenatal diagnosis in the fetal hyperechogenic kidneys: assessment using chromosomal microarray analysis and exome sequencingNARA Subscribed
Human Genetics · 2023 · Vol. 142 · Issue 6 · Springer
Ruibin Huang; Fang Fu; Hang Zhou; Lu Zhang; Tingying Lei; Ken Cheng; Shujuan Yan; Fei Guo; You Wang; Chunling Ma; Ru Li; Qiuxia Yu; Qiong Deng; Lushan Li; Xin Yang; Jin Han; Dongzhi Li; Can Liao
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Knockout of ush2a gene in zebrafish causes hearing impairment and late onset rod-cone dystrophyNARA Subscribed
Human Genetics · 2018 · Vol. 137 · Issue 10 · Springer
Shanshan Han; Xiliang Liu; Shanglun Xie; Meng Gao; Fei Liu; Shanshan Yu; Peng Sun; Changquan Wang; Stephen Archacki; Zhaojing Lu; Xuebin Hu; Yayun Qin; Zhen Qu; Yuwen Huang; Yuexia Lv; Jiayi Tu; Jingzhen Li; Tinsae Assefa Yimer; Tao Jiang; Zhaohui Tang; Daji Luo; Fangyi Chen; Mugen Liu
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A genetic variant in the placenta-derived MHC class I chain-related gene A increases the risk of preterm birth in a Chinese populationNARA Subscribed
Human Genetics · 2017 · Vol. 136 · Issue 10 · Springer
Junjiao Song; Jing Li; Han Liu; Yuexin Gan; Yang Sun; Min Yu; Yongjun Zhang; Fei Luo; Ying Tian; Weiye Wang; Jun Zhang; Julian Little; Haidong Cheng; Dan Chen
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Digenic inheritance of non-syndromic deafness caused by mutations at the gap junction proteins Cx26 and Cx31NARA Subscribed
Human Genetics · 2009 · Vol. 125 · Issue 1 · Springer
Xue-Zhong Liu; Yongyi Yuan; Denise Yan; Emilie Hong Ding; Xiao Mei Ouyang; Yu Fei; Wenxue Tang; Huijun Yuan; Qing Chang; Li Lin Du; Xin Zhang; Guojian Wang; Shoeb Ahmad; Dong Yang Kang; Xi Lin; Pu Dai
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