Heterozygous mutations of FREM1 are associated with an increased risk of isolated metopic craniosynostosis in humans and mice.
, 2011 Sep: 7(9)e1002278
Facial suture synostosis of newborn Fgfr1(P250R/+) and Fgfr2(S252W/+) mouse models of Pfeiffer and Apert syndromes.
Birth defects research. Part A, Clinical and molecular teratology
, July 2011: 91(7)603-9
Manitoba-oculo-tricho-anal (MOTA) syndrome is caused by mutations in FREM1.
Journal of medical genetics
, 2011 Jun: 48(6)375-82
A landmark-free framework for the detection and description of shape differences in embryos.
Conference proceedings : ... Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Conference
, 2011: 20115153-6
Maternal ethanol consumption alters the epigenotype and the phenotype of offspring in a mouse model.
, 2010 Jan 15: 6(1)e1000811