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11. Ellis-van Creveld syndrome in a Western Australian aboriginal community. Postaxial polydactyly as a heterozygous manifestation? Goldblatt J; Minutillo C; Pemberton PJ; Hurst J Med J Aust; 1992 Aug; 157(4):271-2. PubMed ID: 1435447 [TBL] [Abstract][Full Text] [Related]
12. Oral manifestations in Ellis-van Creveld syndrome: report of five cases. Cahuana A; Palma C; Gonzáles W; Geán E Pediatr Dent; 2004; 26(3):277-82. PubMed ID: 15185812 [TBL] [Abstract][Full Text] [Related]
13. Dwarfism in the newborn: the nomenclature, radiological features and genetic significance. Cremin BJ; Beighton P Br J Radiol; 1974 Feb; 47(554):77-93. PubMed ID: 4206212 [No Abstract] [Full Text] [Related]
14. Ellis-van Creveld syndrome. A report of previously undescribed anomalies in two siblings. Blackburn MG; Belliveau RE Am J Dis Child; 1971 Sep; 122(3):267-70. PubMed ID: 5568596 [No Abstract] [Full Text] [Related]
15. A NOVEL MUTATION ASSOCIATED WITH NEPHROLITIHASIS IN ELLIS-VAN CREVELD SYNDROME. Kiraz A; Akin MA; Arslan A; Zabel B; Lausch E Genet Couns; 2015; 26(3):377-9. PubMed ID: 26625674 [No Abstract] [Full Text] [Related]
16. Symptomatic heterozygosity in the Ellis-van Creveld syndrome? Spranger S; Tariverdian G Clin Genet; 1995 Apr; 47(4):217-20. PubMed ID: 7628126 [TBL] [Abstract][Full Text] [Related]