Associated Papers
Results from Genetic Studies in Patients Affected with Craniosynostosis: Clinical and Molecular Aspects.
Bukowska-Olech E et al.
Frontiers in Molecular Biosciences, 2022
Mild nasal malformations and parietal foramina caused by homozygous ALX4 mutations.
Kayserili H et al.
American Journal of Medical Genetics. Part A, 2012
Frontorhiny, a distinctive presentation of frontonasal dysplasia caused by recessive mutations in the ALX3 homeobox gene.
Twigg SR et al.
American Journal of Human Genetics, 2009
Select a paper to view details