Microphthalmia, linear skin defects, callosal agenesis, and cleft palate in a patient with deletion at Xp22.3p22.2 - Pittoli, Siulan Vendramini Paulovich; Souza, Rosana Maria Candido; Quiezi, Rodrigo Gonçalves; Zechi-Ceide, Roseli Maria; Nakata, Nancy Mizue Kokitsu; Jehee, Fernanda Sarquis; Ribeiro-Bicudo, Lucilene Arilho; FitzPatrick, David R.; Guion-Almeida, Maria Leine; Richieri-Costa, Antonio (Journal of Pediatric Genetics, 2020)