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13816810.2013.835432
13816810.2013.835432
http://dx.doi.org/10.3109/13816810.2013.835432
A case of 22q11.2 deletion syndrome with Peters anomaly, congenital glaucoma, and heterozygous mutation in CYP1B1
P356
Q33882393-7BE79CB5-9954-43B0-B735-803A30A90816
P356
13816810.2013.835432
http://dx.doi.org/10.3109/13816810.2013.835432