Palavra-chave: 22Q11.2 DELETION

8P23.1 DELETION SYNDROME SÍNDROME DA DELEÇÃO 22Q11.2 CONGENITAL HEART DISEASE ARRAY GENOMIC HYBRIDIZATION 22Q11.2 DISTAL DUPLICATION GENOTYPE?PHENOTYPE CORRELATION PHENOTYPE 22Q11.2 DELETION SYNDROME DESEQUILÍBRIOS GENÔMICOS COPY NUMBER VARIATIONS CNV MULTIPLEX-LIGATION DEPENDENT PROBE AMPLIFICATION FENDA PALATAL SUBMUCOSA FENDA PALATAL OCULOAURICULOVERTEBRAL SPECTRUM MICROSSOMIA CRANIOFACIAL DISTAL 22Q11.2 DELETION BEHAVIORAL PROBLEMS. ABERRAÇÃO CROMOSSÔMICA GENOTYPE-PHENOTYPE CORRELATION ATYPICAL COPY NUMBER ABNORMALITIES AGH PRMD9 POLIMORPHISM