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Orvosi Hetilap 1

Showing records 1 to 1 | Display all abstracts in Orvosi Hetilap

58921 Homozygous E387K (1159G>A) mutation of the CYP1B1 gene in a Roma boy affected with primary congenital glaucoma. Case report
Vogt G; Kádasi ĽL; Czeizel E
Orvosi Hetilap 2014; 155: 1325-1328

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