HuGE Literature Finder
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Exome sequencing identifies rare variants in multiple genes in atrioventricular septal defect. Genetics in medicine : official journal of the American College of Medical Genetics 2015 May . D'Alessandro Lisa C A, Al Turki Saeed, Manickaraj Ashok Kumar, Manase Dorin, Mulder Barbara J M, Bergin Lynn, Rosenberg Herschel C, Mondal Tapas, Gordon Elaine, Lougheed Jane, Smythe John, Devriendt Koen, Bhattacharya Shoumo, Watkins Hugh, Bentham Jamie, Bowdin Sarah, Hurles Matthew E, Mital See |
Identification of novel significant variants of ZFPM2/FOG2 in non-syndromic Tetralogy of Fallot and double outlet right ventricle in a Chinese Han population. Molecular biology reports 2014 41 (4): 2671-7. Huang Xiaomin, Niu Wenquan, Zhang Zhen, Zhou Chunxia, Xu Zhiwei, Liu Jinfen, Su Zhaokang, Ding Wenxiang, Zhang Hai |
Novel missense variants of ZFPM2/FOG2 identified in conotruncal heart defect patients do not impair interaction with GATA4. PloS one 2014 9 (7): e102379. Zhang Wenwen, Shen Li, Deng Zhantao, Ding Yibing, Mo Xuming, Xu Zhengfeng, Gao Qian, Yi Lo |
New mutations in ZFPM2/FOG2 gene in tetralogy of Fallot and double outlet right ventricle. Clinical genetics 2011 Aug 80 (2): 184-90. De Luca Alessandro, Sarkozy A, Ferese R, Consoli F, Lepri F, Dentici M L, Vergara P, De Zorzi A, Versacci P, Digilio M C, Marino B, Dallapiccola |
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