Exclusion of mutations in TGIF, ALX3, and ALX4 genes in patients with the syndrome of frontonasal dysgenesis, callosal agenesis, basal encephalocele, and eye anomalies - Ribeiro-Bicudo, Lucilene Arilho; Quiezi, Rodrigo Gonçalves; Guion-Almeida, Maria Leine; Legnaro, Chiara; Richieri-Costa, Antonio (American Journal of Medical Genetics, Part A, 2012)