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1-q22.1 (1) 1
abnormalities, multiple - genetics (1) 1
abnormalities, multiple - pathology (1) 1
analysis (1) 1
anomalies (1) 1
array comparative genomic hybridization (1) 1
child, preschool (1) 1
chromosome deletion (1) 1
chromosome-2 (1) 1
chromosomes (1) 1
chromosomes, human, pair 2 - genetics (1) 1
comparative genomic hybridization (1) 1
cytogenetics (1) 1
deficiency (1) 1
deletion 2q14 (1) 1
deletion 2q14.1-q22.1 (1) 1
deletion 2q14.1–q22.1 (1) 1
developmental disabilities - genetics (1) 1
developmental disabilities - pathology (1) 1
disorder (1) 1
dysmorphic features (1) 1
echocardiography (1) 1
gene (1) 1
genetic aspects (1) 1
genetics & heredity (1) 1
gli2 (1) 1
humans (1) 1
index medicus (1) 1
karyotype (1) 1
locus (1) 1
long arm (1) 1
male (1) 1
mutations (1) 1
phenotype (1) 1
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