Figure 3From: A rare de novo duplication of chromosome 21q22.12 → q22.3 with other concomitant deletion and duplication of small fragments in 21q associated with Down syndrome: Prenatal diagnosis, molecular cytogenetic characterizationaCGH results indicated there were three duplications and one deletion in 21q. The largest duplicated region of 11.74 Mb extending from 21q22.12 to 21q22.3, which should contribute to the fetus clinical characterization of Down syndrome.Back to article page