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Ophthalmic Genetics 1

Showing records 1 to 1 | Display all abstracts in Ophthalmic Genetics

27525 A case report of a patient with Pfeiffer syndrome, an FGRF 2 mutation (Trp290Cys) and unique ocular anterior segment findings
Barry GP; Ny BM-L; Zackai EH; Grunwald L; Forbes BJ
Ophthalmic Genetics 2010; 31: 193-195

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