Palavra-chave: 22Q11.2 DELETION

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