Tartaglia M. et al "Jackson-Weiss syndrome: identification of two novel FGFR2 missense mutations shared with Crouzon and Pfeiffer craniosynostotic disorders"   Hum Genet. 1997 Nov;101(1):47-50
Jackson CE. et al "Craniosynostosis, midfacial hypoplasia and foot abnormalities: an autosomal dominant phenotype in a large Amish kindred"   J Pediatr. 1976 Jun;88(6):963-8
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