Delineation of a de novo 7q21.3q31.1 Deletion by CGH-SNP Arrays in a Girl with Multiple Congenital Anomalies Including Severe Glaucoma

Por Martínez-Jacobo, L., Córdova-Fletes, C., Ortiz-López, R., Rivas, F., Saucedo-Carrasco, C., Rojas-Martínez, A.
Publicado em 2013

A de novo sSMC(22) Characterized by High-Resolution Arrays in a Girl with Cat-Eye Syndrome without Coloboma

Por Córdova-Fletes, C., Domínguez, M.G., Vázquez-Cárdenas, A., Figuera, L.E., Neira, V.A., Rojas-Martínez, A., Ortiz-López, R.
Publicado em 2012