A case report of a patient with Pfeiffer syndrome, an FGRF 2 mutation (Trp290Cys) and unique ocular anterior segment findings
Barry, Gerard P., Ny, Betina Mucha-Le, Zackai, Elaine H., Grunwald, Lili, Forbes, Brian J.Volume:
31
Language:
english
Journal:
Ophthalmic Genetics
DOI:
10.3109/13816810.2010.505225
Date:
December, 2010
File:
PDF, 627 KB
english, 2010