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4. Ocular, cerebral and cutaneous malformations: confirmation of an association. Ferguson JW; Hutchison HT; Rouse BM Clin Genet; 1984 May; 25(5):464-9. PubMed ID: 6426831 [TBL] [Abstract][Full Text] [Related]
5. A case in the spectrum of the oculo-encephalo-hepato-renal syndrome. Ehara H; Tamaoki Y; Eda I Pediatr Neurol; 1999 Oct; 21(4):757-62. PubMed ID: 10580893 [TBL] [Abstract][Full Text] [Related]
6. [De Barsy-Moens-Dierckx syndrome: unusual course in a neonate]. Schierenberg M; Donné W; Schiafone P; Bald R; Gembruch U; Hansmann M; Rister M Klin Padiatr; 1994; 206(6):444-6. PubMed ID: 7823530 [TBL] [Abstract][Full Text] [Related]
9. Oculocerebrocutaneous syndrome (Dellman) in an adult. Baruchin AM; Nahlieli O Pediatr Dermatol; 2000; 17(4):333. PubMed ID: 10990594 [No Abstract] [Full Text] [Related]
10. The oculocerebrocutaneous (Delleman) syndrome. al-Gazali LI; Donnai D; Berry SA; Say B; Mueller RF J Med Genet; 1988 Nov; 25(11):773-8. PubMed ID: 3148726 [No Abstract] [Full Text] [Related]
11. Oculo-cerebro-cutaneous syndrome: description of a new case. Giorgi PL; Gabrielli O; Catassi C; Coppa GV Eur J Pediatr; 1989 Jan; 148(4):325-6. PubMed ID: 2707277 [TBL] [Abstract][Full Text] [Related]
12. A novel GJA 1 mutation in oculo-dento-digital dysplasia with curly hair and hyperkeratosis. Kelly SC; Ratajczak P; Keller M; Purcell SM; Griffin T; Richard G Eur J Dermatol; 2006; 16(3):241-5. PubMed ID: 16709485 [TBL] [Abstract][Full Text] [Related]
20. 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] [Next] [New Search]