Skip to main content
. 2024 Apr 17;10(9):e29816. doi: 10.1016/j.heliyon.2024.e29816

Fig. 4.

Fig. 4

Genome sequencing of case 2. The red box show the detection of the variant sites. The RUNX2:c.911-914delinsTTT heterozygous mutation was detected in the fetus, while both the father and mother harbored the wild-type RUNX2 gene.