Ercoli, G; Bidondo, MP; Senra, BC; Groisman, B (September 2014). "Apert syndrome with omphalocele: a case report". Birth Defects Research Part A: Clinical and Molecular Teratology. 100 (9): 726–729. doi:10.1002/bdra.23270. PMID25045033.
Wilkie, A O; S F Slaney; M Oldridge; M D Poole; G J Ashworth; A D Hockley; R D Hayward; D J David; L J Pulleyn; P Rutland (February 1995). "Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome". Nature Genetics. 9 (2): 165–72. doi:10.1038/ng0295-165. PMID7719344. S2CID12423131.
Moloney, DM; Slaney, SF; Oldridge, M; Wall, SA; Sahlin, P; Stenman, G; Wilkie, AO (1996). "Exclusive paternal origin of new mutations in Apert syndrome". Nature Genetics. 13 (1): 48–53. doi:10.1038/ng0596-48. PMID8673103. S2CID26465362.
Britto, J A; J C T Chan; R D Evans; R D Hayward; B M Jones (May 2001). "Differential expression of fibroblast growth factor receptors in human digital development suggests common pathogenesis in complex acrosyndactyly and craniosynostosis". Plastic and Reconstructive Surgery. 107 (6): 1331–1338. doi:10.1097/00006534-200105000-00001. PMID11335797. S2CID32124914.
Ercoli, G; Bidondo, MP; Senra, BC; Groisman, B (September 2014). "Apert syndrome with omphalocele: a case report". Birth Defects Research Part A: Clinical and Molecular Teratology. 100 (9): 726–729. doi:10.1002/bdra.23270. PMID25045033.
Wilkie, A O; S F Slaney; M Oldridge; M D Poole; G J Ashworth; A D Hockley; R D Hayward; D J David; L J Pulleyn; P Rutland (February 1995). "Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome". Nature Genetics. 9 (2): 165–72. doi:10.1038/ng0295-165. PMID7719344. S2CID12423131.
Conrady, Christopher D.; Patel, Bhupendra C.; Sharma, Sandeep (2022), "Apert Syndrome", StatPearls, Treasure Island (FL): StatPearls Publishing, PMID30085535, retrieved 21 September 2022
Moloney, DM; Slaney, SF; Oldridge, M; Wall, SA; Sahlin, P; Stenman, G; Wilkie, AO (1996). "Exclusive paternal origin of new mutations in Apert syndrome". Nature Genetics. 13 (1): 48–53. doi:10.1038/ng0596-48. PMID8673103. S2CID26465362.
Britto, J A; J C T Chan; R D Evans; R D Hayward; B M Jones (May 2001). "Differential expression of fibroblast growth factor receptors in human digital development suggests common pathogenesis in complex acrosyndactyly and craniosynostosis". Plastic and Reconstructive Surgery. 107 (6): 1331–1338. doi:10.1097/00006534-200105000-00001. PMID11335797. S2CID32124914.
Wilkie, A O; S F Slaney; M Oldridge; M D Poole; G J Ashworth; A D Hockley; R D Hayward; D J David; L J Pulleyn; P Rutland (February 1995). "Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome". Nature Genetics. 9 (2): 165–72. doi:10.1038/ng0295-165. PMID7719344. S2CID12423131.
Moloney, DM; Slaney, SF; Oldridge, M; Wall, SA; Sahlin, P; Stenman, G; Wilkie, AO (1996). "Exclusive paternal origin of new mutations in Apert syndrome". Nature Genetics. 13 (1): 48–53. doi:10.1038/ng0596-48. PMID8673103. S2CID26465362.
Britto, J A; J C T Chan; R D Evans; R D Hayward; B M Jones (May 2001). "Differential expression of fibroblast growth factor receptors in human digital development suggests common pathogenesis in complex acrosyndactyly and craniosynostosis". Plastic and Reconstructive Surgery. 107 (6): 1331–1338. doi:10.1097/00006534-200105000-00001. PMID11335797. S2CID32124914.