. . . . . "SPECC1L" . . . . "Mutations in SPECC1L, encoding sperm antigen with calponin homology and coiled-coil domains 1-like, are found in some cases of autosomal dominant Opitz G/BBB syndrome." . . . . "2018-04-05T10:17:11.353+02:00"^^ . . . . . .