MAMLD1 Gene Mutation in the Incidence of Hypospadias in the Chinese Population

by Zhuang Likai, Bai Ming, Zhou Wei, Yu Yongguo, Wang Jian, Fu Qihua, Sun Jie
Published 2014-09-01

Molecular Characteristic and Virulence Gene Profiles of Community-Associated Methicillin-Resistant Staphylococcus aureus Isolates from Pediatric Patients in Shanghai, China

by Wang, Xing, Li, Xia, Liu, Wei, Huang, Weichun, Fu, Qihua, Li, Min
Published 2016

Investigation of Somatic NKX2-5 Mutations in Chinese Children with Congenital Heart Disease

by Zheng, Jiayi, Li, Fen, Liu, Jinfen, Xu, Zhiwei, Zhang, Haibo, Fu, Qihua, Wang, Jian, Sun, Kun
Published 2015

A modified multiplex ligation-dependent probe amplification method for the detection of 22q11.2 copy number variations in patients with congenital heart disease

by Zhang, Xiaoqing, Xu, Yuejuan, Liu, Deyuan, Geng, Juan, Chen, Sun, Jiang, Zhengwen, Fu, Qihua, Sun, Kun
Published 2015

A Novel Missense Mutation of GATA4 in a Chinese Family with Congenital Heart Disease

by Zhang, Xiaoqing, Wang, Jian, Wang, Bo, Chen, Sun, Fu, Qihua, Sun, Kun
Published 2016

Novel Mutations in the SCNN1A Gene Causing Pseudohypoaldosteronism Type 1

by Wang, Jian, Yu, Tingting, Yin, Lei, Li, Jing, Yu, Li, Shen, Ye, Yu, Yongguo, Shen, Yongnian, Fu, Qihua
Published 2013

Causal variants screened by whole exome sequencing in a patient with maternal uniparental isodisomy of chromosome 10 and a complicated phenotype

by LI, NIU, DING, YU, YU, TINGTING, LI, JUAN, SHEN, YONGNIAN, WANG, XIUMIN, FU, QIHUA, SHEN, YIPING, HUANG, XIAODONG, WANG, JIAN
Published 2016

The Fas/Fas Ligand Death Receptor Pathway Contributes to Phenylalanine-Induced Apoptosis in Cortical Neurons

by Huang, Xiaodong, Lu, Zhaohui, Lv, Zhongwei, Yu, Tingting, Yang, Peirong, Shen, Yongnian, Ding, Yu, Fu, Da, Zhang, Xiaoping, Fu, Qihua, Yu, Yongguo
Published 2013

Screening for Coding Variants in FTO and SH2B1 Genes in Chinese Patients with Obesity

by Zheng, Zhaojing, Hong, Li, Huang, Xiaodong, Yang, Peirong, Li, Juan, Ding, Yu, Yao, Ru-en, Geng, Juan, Shen, Yongnian, Shen, Yiping, Fu, Qihua, Yu, Yongguo
Published 2013

Chromosome microarray testing for patients with congenital heart defects reveals novel disease causing loci and high diagnostic yield

by Geng, Juan, Picker, Jonathan, Zheng, Zhaojing, Zhang, Xiaoqing, Wang, Jian, Hisama, Fuki, Brown, David W, Mullen, Mary P, Harris, David, Stoler, Joan, Seman, Ann, Miller, David T, Fu, Qihua, Roberts, Amy E, Shen, Yiping
Published 2014