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Williamson K 1
Showing records 1 to 1 | Display all abstracts from Williamson K18540 PAX6 mutation in a family with aniridia, congenital ptosis, and mental retardation
Malandrini A; Mari F; Palmeri S; Gambelli S; Berti G; Bruttini M; Bardelli AM; Williamson K; van Heyningen V; Renieri A
Clinical Genetics 2001; 60: 151-154
