Delineation of a de novo 7q21.3q31.1 deletion by CGH-SNP arrays in a girl with multiple congenital anomalies including severe glaucoma

L. Martínez-Jacobo, C. Córdova-Fletes, R. Ortiz-López, F. Rivas, C. Saucedo-Carrasco, A. Rojas-Martínez

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