Fig. 3From: Intragenic microdeletion of RUNX2 is a novel mechanism for cleidocranial dysplasiaAnalysis of RUNX2 copy number using RT-qPCR. Copy number of RUNX2 was determined for all the exons and 3′UTR. I:2, I:5, I:8, II:1, II:5, II:8, III:1, III:2 were patients and II:2 and II:6 were controls from the CCD extended family. S1 was a sporadic caseBack to article page