| bibliographicCitation |
Dines JN, Liu YJ, Neufeld‐Kaiser W, Sawyer T, Ishak GE, Tully HM, Racobaldo M, Sanchez‐Valle A, Disteche CM, Juusola J, Torti E, McWalter K, Doherty D, Dipple KM. Expanding phenotype with severe midline brain anomalies and missense variant supports a causal role for FOXA2 in 20p11.2 deletion syndrome. American J of Med Genetics Pt A. 2019 Jul 11;179(9):1783–90. doi: 10.1002/ajmg.a.61281. |