Síndrome de Apert (Spanish Wikipedia)

Analysis of information sources in references of the Wikipedia article "Síndrome de Apert" in Spanish language version.

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  • 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 genetics 9 (2): 165-72. PMID 7719344. doi:10.1038/ng0295-165. 
  • Goriely, A.; McVean, GA; Röjmyr, M; Ingemarsson, B; Wilkie, AO (2003). «Evidence for Selective Advantage of Pathogenic FGFR2 Mutations in the Male Germ Line». Science 301 (5633): 643-6. PMID 12893942. 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 genetics 13 (1): 48-53. PMID 8673103. doi:10.1038/ng0596-48. 

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