https://pubmed.ncbi.nlm.nih.gov/7719344/
Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome
Apert syndrome is a distinctive human malformation comprising craniosynostosis and severe syndactyly of the hands and feet. We have identified specific...
https://www.ebsco.com/research-starters/health-and-medicine/crouzon-syndrome
Crouzon syndrome | Health and Medicine | Research Starters | EBSCO Research
health and medicine researchcrouzon syndromestartersebsco