Condition: PARIETAL FORAMINA 1
rs104893896
in
MSX2
gene and
PARIETAL FORAMINA 1
PMID 10767351
2000 Identification of mutations in the MSX2 homeobox gene in families affected with foramina parietalia permagna.
PMID 10742103
2000 Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossification.