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000353510
000353510
http://dx.doi.org/10.1159/000353510
Delineation of a de novo 7q21.3q31.1 Deletion by CGH-SNP Arrays in a Girl with Multiple Congenital Anomalies Including Severe Glaucoma.
P356
Q37180729-CB4724EF-6293-4265-A4C6-368AE80D8743
P356
000353510
http://dx.doi.org/10.1159/000353510