Palavra-chave: 22Q11.2 DELETION

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