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Springer Nature5
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✓Human Genetics5
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20232
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Cheng Fu results 5 · Newest (Page 1/1, per page 25)
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Journal: Human Genetics ×Author: Cheng Fu ×Clear All Filters
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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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Whole exome sequencing improves genetic diagnosis of fetal clubfootNARA Subscribed
Human Genetics · 2023 · Vol. 142 · Issue 3 · Springer
Ruibin Huang; Hang Zhou; Chunling Ma; Fang Fu; Ken Cheng; You Wang; Ru Li; Tingying Lei; Qiuxia Yu; Dan Wang; Shujuan Yan; Xin Yang; Dongzhi Li; Can Liao
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Loss-of-function mutation in the X-linked TBX22 promoter disrupts an ETS-1 binding site and leads to cleft palateNARA Subscribed
Human Genetics · 2015 · Vol. 134 · Issue 2 · Springer
Xiazhou Fu; Yibin Cheng; Jia Yuan; Chunhua Huang; Hanhua Cheng; Rongjia Zhou
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Significant association of SNP rs2106261 in the ZFHX3 gene with atrial fibrillation in a Chinese Han GeneID populationNARA Subscribed
Human Genetics · 2011 · Vol. 129 · Issue 3 · Springer
Cong Li; Fan Wang; Yanzong Yang; Fenfen Fu; Chengqi Xu; Lisong Shi; Sisi Li; Yunlong Xia; Gang Wu; Xiang Cheng; Hui Liu; Chuchu Wang; Pengyun Wang; Jianjun Hao; Yuhe Ke; Yuanyuan Zhao; Mugen Liu; Rongfeng Zhang; Lianjun Gao; Bo Yu; Qiutang Zeng; Yuhua Liao; Bo Yang; Xin Tu; Qing K. Wang
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Small heat-shock protein 22 mutated in autosomal dominant Charcot-Marie-Tooth disease type 2LNARA Subscribed
Human Genetics · 2005 · Vol. 116 · Issue 3 · Springer
Bei-sha Tang; Guo-hua Zhao; Wei Luo; Kun Xia; Fang Cai; Qian Pan; Ru-xu Zhang; Fu-feng Zhang; Xiao-min Liu; Biao Chen; Cheng Zhang; Lu Shen; Hong Jiang; Zhi-gao Long; He-ping Dai
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