(Q34623067)
Statements
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A case report of a patient with Pfeiffer syndrome, an FGRF 2 mutation (Trp290Cys) and unique ocular anterior segment findings (English)
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Gerard P Barry
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Betina Mucha-Le Ny
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Elaine H Zackai
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Lili Grunwald
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Brian J Forbes
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1 September 2010
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Identifiers
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