Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Tetralogy of Fallot and GDF1[original query] |
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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 |
Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands. Nature genetics 2017 10 49 (11): 1593-1601. Jin Sheng Chih, Homsy Jason, Zaidi Samir, Lu Qiongshi, Morton Sarah, DePalma Steven R, Zeng Xue, Qi Hongjian, Chang Weni, Sierant Michael C, Hung Wei-Chien, Haider Shozeb, Zhang Junhui, Knight James, Bjornson Robert D, Castaldi Christopher, Tikhonoa Irina R, Bilguvar Kaya, Mane Shrikant M, Sanders Stephan J, Mital Seema, Russell Mark W, Gaynor J William, Deanfield John, Giardini Alessandro, Porter George A, Srivastava Deepak, Lo Cecelia W, Shen Yufeng, Watkins W Scott, Yandell Mark, Yost H Joseph, Tristani-Firouzi Martin, Newburger Jane W, Roberts Amy E, Kim Richard, Zhao Hongyu, Kaltman Jonathan R, Goldmuntz Elizabeth, Chung Wendy K, Seidman Jonathan G, Gelb Bruce D, Seidman Christine E, Lifton Richard P, Brueckner Marti |
Association of functional variant in GDF1 promoter with risk of congenital heart disease and its regulation by Nkx2.5. Clinical science (London, England : 1979) 2019 Jun . Gao Xiaobo, Zheng Panpan, Yang Liping, Luo Haiyan, Zhang Chen, Qiu Yongqiang, Huang Guoying, Sheng Wei, Ma Xu, Lu Caili |
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- Page last updated:Sep 18, 2023
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