These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
27. Fraser syndrome and cryptophthalmos: review of the diagnostic criteria and evidence for phenotypic modules in complex malformation syndromes. Slavotinek AM; Tifft CJ J Med Genet; 2002 Sep; 39(9):623-33. PubMed ID: 12205104 [TBL] [Abstract][Full Text] [Related]
28. [Fraser syndrome: frequency in our environment and clinical-epidemiological aspects of a consecutive series of cases]. Martínez-Frías ML; Bermejo Sánchez E; Félix V; Calvo Celada R; Ayala Garcés A; Hernández Ramón F An Esp Pediatr; 1998 Jun; 48(6):634-8. PubMed ID: 9662850 [TBL] [Abstract][Full Text] [Related]
29. Asphyxiating thoracic dystrophy and syndactyly of the toes in a newborn: coincidence or a new association? Tastekin A; Polat P; Ors R Genet Couns; 2003; 14(1):113-4. PubMed ID: 12725597 [No Abstract] [Full Text] [Related]
30. Oculo-dento-digital dysplasia (OMIM *164200). Full manifestation of the syndrome in a 9.5 year-old girl and type III syndactyly in the father. Ioan DM; Dagomiz D; Fryns JP Genet Couns; 2002; 13(2):187-9. PubMed ID: 12150221 [TBL] [Abstract][Full Text] [Related]
31. Novel GJA1 mutations in patients with oculo-dento-digital dysplasia (ODDD). Debeer P; Van Esch H; Huysmans C; Pijkels E; De Smet L; Van de Ven W; Devriendt K; Fryns JP Eur J Med Genet; 2005; 48(4):377-87. PubMed ID: 16378922 [TBL] [Abstract][Full Text] [Related]
32. Mental retardation, obesity, mandibular prognathism with eye and skin anomalies (MOMES syndrome): a newly recognized autosomal recessive syndrome. Kantaputra PN; Kunachaichote J; Patikulsila P Am J Med Genet; 2001 Nov; 103(4):283-8. PubMed ID: 11746007 [TBL] [Abstract][Full Text] [Related]
33. Central nervous system abnormalities in oculodentodigital dysplasia. Schrander-Stumpel CT; Franke CL Genet Couns; 1996; 7(3):233-5. PubMed ID: 8897047 [No Abstract] [Full Text] [Related]
34. Neonatal death in Marshall-Smith syndrome. Chatel C; Maazoul F; Sigaudy S; Fredouille C; Ayme S; Philip N Genet Couns; 1998; 9(1):15-8. PubMed ID: 9555581 [TBL] [Abstract][Full Text] [Related]