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

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

• Book ID: 121009424
• Publisher: S. Karger AG
• Year: 2013
• Tongue: English
• Weight: 292 KB
• Category: Article
• ISSN: 1661-8769
• DOI: 10.1159/000353510