Repositorio de Universidad Autónoma de Chile.
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Association between phenotype and deletion size in 22q11.2 microdeletion syndrome: Systematic review and meta-analysis
Background: Chromosome 22q11.2 microdeletion syndrome, a disorder caused by heterozygous loss of genetic material in chromosome region 22q11.2, has a broad range of clinical symptoms. The most common congenital anomalies involve the palate in 80% of patients, and the heart in 50-60% of them. The cau
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