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Identification of novel FBN1 variations implicated in congenital scoliosis
Lin, Mao, Zhao, Sen, Liu, Gang, Huang, Yingzhao, Yu, Chenxi, Zhao, Yanxue, Wang, Lianlei, Zhang, Yuanqiang, Yan, Zihui, Wang, Shengru, Liu, Sen, Liu, Jiaqi, Ye, Yongyu, Chen, Yaping, Yang, Xu, Tong, Bingdu, Wang, Zheng, Yang, Xinzhuang, Niu, Yuchen, Li, Xiaoxin, Wang, Yipeng, Su, Jianzhong, Yuan, Jian, Zhao, Hengqiang, Zhang, Shuyang, Qiu, Guixing, Wu, Zhihong, Zhang, Jianguo, Wu, Nan, Zuo, Yuzhi, Ikegawa, Shiro, Wu, Nan
Published in Journal of human genetics (01.03.2020)
Published in Journal of human genetics (01.03.2020)
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Journal Article
An integrated clinical and molecular study of a cohort of Turkish patients with Marfan syndrome harboring known and novel FBN1 variants
Gezdirici, Alper, Teralı, Kerem, Gülec, Elif Yılmaz, Bornaun, Helen, Dogan, Mustafa, Eröz, Recep
Published in Journal of human genetics (01.07.2021)
Published in Journal of human genetics (01.07.2021)
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Journal Article