Description of a new mutation and caracterization of FGFR1, FGFR2, and FGFR3 mutations among Brazilian patients with syndromic craniosynostoses - Passos-Bueno, Maria Rita; Sertié, Andréa L; Richieri-Costa, Antonio; Alonso, Luís G; Zatz, Mayana; Alonso, Nivaldo; Brunoni, Decio; Ribeiro, Sandra F M (American Journal of Medical Genetics, 1998)