Palavra-chave: 22Q11.2 DELETION

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