Associated Papers
Novel FGFR2 deletion in a patient with Beare-Stevenson-like syndrome.
Slavotinek A et al.
American Journal of Medical Genetics. Part A, 2009
Genetics of craniosynostosis: genes, syndromes, mutations and genotype-phenotype correlations.
Passos-Bueno MR et al.
Frontiers of Oral Biology, 2008
Bad bones, absent smell, selfish testes: the pleiotropic consequences of human FGF receptor mutations.
Wilkie AO
Cytokine & Growth Factor Reviews, 2005
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