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Schilter KF 1
Showing records 1 to 1 | Display all abstracts from Schilter KF50347 PITX2 and FOXC1 spectrum of mutations in ocular syndromes
Reis LM; Tyler RC; Volkmann Kloss BA; Schilter KF; Levin AV; Lowry RB; Zwijnenburg PJ; Stroh E; Broeckel U; Murray JC; Semina EV
European Journal of Human Genetics 2012; 20: 1224-1233