Синдром Аперта (Russian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Синдром Аперта" in Russian 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. Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome (англ.) // Nature genetics : journal. — 1995. — February (vol. 9, no. 2). — P. 165—172. — doi:10.1038/ng0295-165. — PMID 7719344.

neuro-online.ru

nih.gov

ncbi.nlm.nih.gov

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