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Goriely, A.; McVean, GA; Röjmyr, M; Ingemarsson, B; Wilkie, AO (2003). «Evidence for Selective Advantage of Pathogenic FGFR2 Mutations in the Male Germ Line». Science301 (5633): 643-6. PMID12893942. doi:10.1126/science.1085710.
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 genetics13 (1): 48-53. PMID8673103. doi:10.1038/ng0596-48.
issn.org
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Fearon, J A (2003-07). «Treatment of the Hands and Feet in Apert Syndrome: An Evolution in Management». Plastic and Reconstructive surgery112 (1): 1-12. ISSN0032-1052. PMID12832871.
Fearon, J A (2003-07). «Treatment of the Hands and Feet in Apert Syndrome: An Evolution in Management». Plastic and Reconstructive surgery112 (1): 1-12. ISSN0032-1052. PMID12832871.
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 (1995-02). «Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome». Nature genetics9 (2): 165-72. PMID7719344. doi:10.1038/ng0295-165.La referencia utiliza el parámetro obsoleto |coautores= (ayuda)
Goriely, A.; McVean, GA; Röjmyr, M; Ingemarsson, B; Wilkie, AO (2003). «Evidence for Selective Advantage of Pathogenic FGFR2 Mutations in the Male Germ Line». Science301 (5633): 643-6. PMID12893942. doi:10.1126/science.1085710.
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 genetics13 (1): 48-53. PMID8673103. doi:10.1038/ng0596-48.