Unique phenotype in a Brazilian girl with syndromic Robin sequence and a 5.6 mb deletion in xp11.4p11.3 - Nakata, Nancy Mizue Kokitsu; Jehee, F; Sandri, R; Pittoli, Siulan Vendramini Paulovich; Alvarez, Camila Wenceslau; Monteiro, R; Mazzeu, J; Zechi-Ceide, Roseli Maria; Richieri-Costa, Antonio (European Cleft Palate Craniofacial Association Congress, 2019)