1. Common genetic causes of holoprosencephaly are limited to a small set of evolutionarily conserved driver genes of midline development coordinated by TGF‐β, hedgehog, and FGF signaling. Issue 10 (26th July 2018) Authors: Roessler, Erich; Hu, Ping; Marino, Juliana; Hong, Sungkook; Hart, Rachel; Berger, Seth; Martinez, Ariel; Abe, Yu; Kruszka, Paul; Thomas, James W.; Mullikin, James C.; Wang, Yupeng; Wong, Wendy S.W.; Niederhuber, John E.; Solomon, Benjamin D.; Richieri‐Costa, Antônio; Ribeiro‐Bicudo, L.A.; Muenke,... Journal: Human mutation Issue: Volume 39:Issue 10(2018) Page Start: 1416 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗