Palavra-chave: 22Q11.2 DELETION

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