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Fig. 2 | Molecular Cytogenetics

Fig. 2

From: Investigation of copy number variations on chromosome 21 detected by comparative genomic hybridization (CGH) microarray in patients with congenital anomalies

Fig. 2

Flow chart of CNVs analysis and corresponding phenotype with OMIM genes. Note: Pink color indicate copy number loss, light green color indicate copy number gain. F = female, M = male, y = year, m = month, d = day, DD = developmental delay

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Molecular Cytogenetics

ISSN: 1755-8166