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52. Variable expressivity of Crouzon's syndrome within a family. Kreiborg S; Jensen BL Scand J Dent Res; 1977 Mar; 85(3):175-84. PubMed ID: 265609 [TBL] [Abstract][Full Text] [Related]
53. [Case of severe neonatal craniofacial dysostosis. Crouzon's syndrome with the aspect of "trefoil cranium"]. Lambotte C; Dodinval P; Beauduin P; Senterre J J Genet Hum; 1974 Dec; 22(4):317-22. PubMed ID: 4461761 [No Abstract] [Full Text] [Related]
54. Calcaneocuboid coalition in Crouzon's syndrome (craniofacial dysostosis): report of a case and review of the literature. Craig CL; Goldberg MJ J Bone Joint Surg Am; 1977 Sep; 59(6):826-7. PubMed ID: 908708 [No Abstract] [Full Text] [Related]
55. A father and son with a nonsevere form of Crouzon's syndrome. Mamikoglu B; Mamikoglu A Ear Nose Throat J; 2000 May; 79(5):368, 371. PubMed ID: 10832202 [TBL] [Abstract][Full Text] [Related]
56. Crouzon's Syndrome: A Rare Genetic Disorder. Kaushik A; Bhatia H; Sharma N Int J Clin Pediatr Dent; 2016; 9(4):384-387. PubMed ID: 28127173 [TBL] [Abstract][Full Text] [Related]
57. FGFR3 gene mutation (Gly380Arg) with achondroplasia and i(21q) Down syndrome: phenotype-genotype correlation. Chen H; Mu X; Sonoda T; Kim KC; Dailey K; Martinez J; Tuck-Muller C; Wertelecki W South Med J; 2000 Jun; 93(6):622-4. PubMed ID: 10881785 [TBL] [Abstract][Full Text] [Related]
58. [Craniofacial dysostosis (Crouzon's syndrome)]. Alves AC Acta Med Port; 1979; 1(1):89-96. PubMed ID: 549466 [No Abstract] [Full Text] [Related]
59. Mutations in fibroblast growth factor receptor 2 gene and craniosynostotic syndromes in Japanese children. Nagase T; Nagase M; Hirose S; Ohmori K J Craniofac Surg; 1998 Mar; 9(2):162-70. PubMed ID: 9586546 [TBL] [Abstract][Full Text] [Related]
60. Central nervous system imaging in Crouzon's syndrome. Proudman TW; Clark BE; Moore MH; Abbott AH; David DJ J Craniofac Surg; 1995 Sep; 6(5):401-5. PubMed ID: 9020723 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]