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Martí,nez-Jacobo L 1

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54850 Delineation of a de novo 7q21.3q31.1 Deletion by CGH-SNP Arrays in a Girl with Multiple Congenital Anomalies Including Severe Glaucoma
Martí,nez-Jacobo L; Có,rdova-Fletes C; Ortiz-Ló,pez R; Rivas F; Saucedo-Carrasco C; Rojas-Martí,nez A
Molecular syndromology 2013; 4: 285-291

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