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7. The Greig cephalopolysyndactyly syndrome: report of a family and review of the literature. Gollop TR, Fontes LR. Am J Med Genet; 1985 Sep; 22(1):59-68. PubMed ID: 3901752 [Abstract] [Full Text] [Related]
9. Hyperphalangism, facial anomalies, hallux valgus, and bronchomalacia: a new syndrome? Chitayat D, Haj-Chahine S, Stalker HJ, Azouz EM, Côté A, Halal F. Am J Med Genet; 1993 Jan 01; 45(1):1-4. PubMed ID: 8418638 [Abstract] [Full Text] [Related]
14. Costello syndrome: the natural history of a true postnatal growth retardation syndrome. Umans S, Decock P, Fryns JP. Genet Couns; 1995 Apr 01; 6(2):121-5. PubMed ID: 7546454 [Abstract] [Full Text] [Related]
15. Opitz-C syndrome: on the nosology of mental retardation and trigonocephaly. Schaap C, Schrander-Stumpel CT, Fryns JP. Genet Couns; 1992 Apr 01; 3(4):209-15. PubMed ID: 1472356 [Abstract] [Full Text] [Related]
16. [Cohen syndrome: report of two cases in female twins]. Arcas Martínez J, García Peñas JJ, Ramos Lizana J, Díaz González C, Pascual Castroviejo I. An Esp Pediatr; 1991 Jan 01; 34(1):83-5. PubMed ID: 2018266 [No Abstract] [Full Text] [Related]
17. Diagnostic criteria for the whistling face syndrome. Antley RM, Uga N, Burzynski NJ, Baum RS, Bixler D. Birth Defects Orig Artic Ser; 1975 Jan 01; 11(5):161-8. PubMed ID: 1218209 [No Abstract] [Full Text] [Related]
18. Antley-Bixler syndrome: case report and review of the literature. Poddevin F, Delobel B, Courreges P, Bayart M. Genet Couns; 1995 Jan 01; 6(3):241-6. PubMed ID: 8588853 [Abstract] [Full Text] [Related]
19. Cohen syndrome. Alavi S, Kher A, Kumar A, Muranjan M, Bharucha B. Indian Pediatr; 1993 May 01; 30(5):678-81. PubMed ID: 8282400 [No Abstract] [Full Text] [Related]