A novel SPECC1L mutation causing Teebi hypertelorism syndrome: Expanding phenotypic and genetic spectrum

Autor: Zhang, Ting, Wu, Qian, Zhu, Ling, Wu, Dingwen, Yang, Rulai, Qi, Ming, Huang, Xinwen
Zdroj: In European Journal of Medical Genetics April 2020 63(4)
Databáze: ScienceDirect