Prenatal diagnosis of fetal thanatophoric dysplasia type 1 with de novo c.2419T > G (p. Ter807Gly) (X807G) gene mutation in fibroblast growth factor receptor 3 (FGFR3) showing increased nuchal translucency at the first trimester of gestation: A case report with review of the literatureMichail Varras, Antonios Kondylios, Eleni Sekerli et al.|Journal of Molecular and Clinical Medicine|2020Cited by 0