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3. Fibroblast growth factor receptor 2 mutations in Beare-Stevenson cutis gyrata syndrome. Przylepa KA; Paznekas W; Zhang M; Golabi M; Bias W; Bamshad MJ; Carey JC; Hall BD; Stevenson R; Orlow S; Cohen MM; Jabs EW Nat Genet; 1996 Aug; 13(4):492-4. PubMed ID: 8696350 [TBL] [Abstract][Full Text] [Related]
4. Somatic FGFR and TWIST mutations are not a common cause of isolated nonsyndromic single suture craniosynostosis. Anderson PJ; Cox TC; Roscioli T; Elakis G; Smithers L; David DJ; Powell B J Craniofac Surg; 2007 Mar; 18(2):312-4. PubMed ID: 17414280 [TBL] [Abstract][Full Text] [Related]
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6. Craniosynostosis syndromes: from genes to premature fusion of skull bones. Hehr U; Muenke M Mol Genet Metab; 1999 Oct; 68(2):139-51. PubMed ID: 10527665 [No Abstract] [Full Text] [Related]
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20. A case of Beare-Stevenson cutis gyrata syndrome confirmed by mutation analysis of the fibroblast growth factor receptor 2 gene. Akai T; Iizuka H; Kishibe M; Kawakami S; Kobayashi A; Ozawa T Pediatr Neurosurg; 2002 Aug; 37(2):97-9. PubMed ID: 12145519 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]