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. 2018 Jan 12;26(3):350–358. doi: 10.1038/s41431-017-0080-4

Fig. 1.

Fig. 1

Pedigrees of the families presented in this study. Individuals who have molecularly confirmed SHOX haploinsufficiency are shaded in black. Individuals with OI type 1 are shaded in grey. Height SDS is shown where available. The arrow in each pedigree indicates the infant in each of our cases presenting in utero with short long bones on routine antenatal scanning