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. 2013 Dec 7;19(3):e248–e254. doi: 10.4317/medoral.19173

Figure 2.

Figure 2

MSX1 MUTATIONS ASSOCIATED WITH DENTAL AGENESIS (HD, homeodomain): 62dupG (44); 182T>A (42); 314C>A (34); 559C>T (43); 587G>C (40); 605C>A, associated with Witkop Syndrom (30).