Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Counseling and GATA4[original query] |
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Prevalence and Spectrum of NKX2-5 Mutations Associated With Sporadic Adult-Onset Dilated Cardiomyopathy. International heart journal 2017 Jul . Xu Jia-Hong, Gu Jian-Yun, Guo Yu-Han, Zhang Hong, Qiu Xing-Biao, Li Ruo-Gu, Shi Hong-Yu, Liu Hua, Yang Xiao-Xiao, Xu Ying-Jia, Qu Xin-Kai, Yang Yi-Qi |
A novel NR2F2 loss-of-function mutation predisposes to congenital heart defect. European journal of medical genetics 2017 12 61 (4): 197-203. Qiao Xiao-Hui, Wang Qian, Wang Juan, Liu Xing-Yuan, Xu Ying-Jia, Huang Ri-Tai, Xue Song, Li Yan-Jie, Zhang Min, Qu Xin-Kai, Li Ruo-Gu, Qiu Xing-Biao, Yang Yi-Qi |
GATA6 loss-of-function mutation contributes to congenital bicuspid aortic valve. Gene 2018 4 663 115-120. Xu Ying-Jia, Di Ruo-Min, Qiao Qi, Li Xiu-Mei, Huang Ri-Tai, Xue Song, Liu Xing-Yuan, Wang Juan, Yang Yi-Qi |
Screening of targeted panel genes in Brazilian patients with primary ovarian insufficiency. PloS one 2020 10 15 (10): e0240795. França Monica M, Funari Mariana F A, Lerario Antonio M, Santos Mariza G, Nishi Mirian Y, Domenice Sorahia, Moraes Daniela R, Costalonga Everlayny F, Maciel Gustavo A R, Maciel-Guerra Andrea T, Guerra-Junior Gil, Mendonca Berenice |
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