Human Genome Epidemiology Literature Finder
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Query Trace: Abnormalities and TBX6[original query] |
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TBX6-associated congenital scoliosis (TACS) as a clinically distinguishable subtype of congenital scoliosis: further evidence supporting the compound inheritance and TBX6 gene dosage model. Genetics in medicine : official journal of the American College of Medical Genetics 2019 1 21 (7): 1548-1558. Liu Jiaqi, Wu Nan, , Yang Nan, Takeda Kazuki, Chen Weisheng, Li Weiyu, Du Renqian, Liu Sen, Zhou Yangzhong, Zhang Ling, Liu Zhenlei, Zuo Yuzhi, Zhao Sen, Blank Robert, Pehlivan Davut, Dong Shuangshuang, Zhang Jianguo, Shen Jianxiong, Si Nuo, Wang Yipeng, Liu Gang, Li Shugang, Zhao Yanxue, Zhao Hong, Chen Yixin, Zhao Yu, Song Xiaofei, Hu Jianhua, Lin Mao, Tian Ye, Yuan Bo, Yu Keyi, Niu Yuchen, Yu Bin, Li Xiaoxin, Chen Jia, Yan Zihui, Zhu Qiankun, Meng Xiaolu, Chen Xiaoli, Su Jianzhong, Zhao Xiuli, Wang Xiaoyue, Ming Yue, Li Xiao, Raggio Cathleen L, Zhang Baozhong, Weng Xisheng, Zhang Shuyang, Zhang Xue, Watanabe Kota, Matsumoto Morio, , Jin Li, Shen Yiping, Sobreira Nara L, Posey Jennifer E, Giampietro Philip F, Valle David, , Liu Pengfei, Wu Zhihong, Ikegawa Shiro, Lupski James R, Zhang Feng, Qiu Guixi |
Prenatal prevalence and postnatal manifestations of 16p11.2 deletions: A new insights into neurodevelopmental disorders based on clinical investigations combined with multi-omics analysis. Clinica chimica acta; international journal of clinical chemistry 2023 11 552 117671. Lan Liu, Jiamin Wang, Xijing Liu, Jing Wang, Lin Chen, Hongmei Zhu, Jingqun Mai, Ting Hu, Shanling L |
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- Page last updated:Apr 22, 2024
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