Human Genome Epidemiology Literature Finder
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Query Trace: Tetralogy of Fallot and TBX20[original query] |
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T-box transcription factor TBX20 mutations in Chinese patients with congenital heart disease. European journal of medical genetics 0 51 (6): 580-7. Liu Caixia, Shen Adong, Li Xiaofeng, Jiao Weiwei, Zhang Xingen, Li Zhongz |
Genetic mutation analysis in Japanese patients with non-syndromic congenital heart disease. Journal of human genetics 2015 Oct . Yoshida Akiko, Morisaki Hiroko, Nakaji Mai, Kitano Masataka, Kim Ki-Sung, Sagawa Koichi, Ishikawa Shiro, Satokata Ichiro, Mitani Yoshihide, Kato Hitoshi, Hamaoka Kenji, Echigo Shigeyuki, Shiraishi Isao, Morisaki Takayu |
Single-Nucleotide Polymorphisms in Exonic and Promoter Regions of Transcription Factors of Second Heart Field Associated with Sporadic Congenital Cardiac Anomalies. Balkan journal of medical genetics : BJMG 2021 Nov 24 (2): 39-47. Wang E, Fan X, Nie Y, Zheng Z, Hu |
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