Phenotypic variability of syndromic craniosynostosis caused by c.833G > T in FGFR2: Clinical and genetic evaluation of eight patients from a five‐generation family

por Wei, Xianda, Huang, Guori, Gui, Baoheng, Xie, Bobo, Chen, Shaoke, Fan, Xin, Chen, Yujun
Publicado 2022