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

Human Mutation, EarlyView.

Source: Human Mutation - July 27, 2018 Category: Genetics & Stem Cells Authors: ErichRoessler , PingHu , JulianaMarino , SungkookHong , RachelHart , SethBerger , ArielMartinez , YuAbe , PaulKruszka , James W.Thomas , James C.Mullikin , , YupengWang , Wendy S.W.Wong , John E.Niederhuber , Benjamin D.Sol Source Type: research