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3. Oculocerebral malformations. A reappraisal of Walker's 'lissencephaly'. Chan CC; Egbert PR; Herrick MK; Urich H Arch Neurol; 1980 Feb; 37(2):104-8. PubMed ID: 6766714 [TBL] [Abstract][Full Text] [Related]
4. Familial lissencephaly with cleft palate and severe cerebellar hypoplasia. Kerner B; Graham JM; Golden JA; Pepkowitz SH; Dobyns WB Am J Med Genet; 1999 Dec; 87(5):440-5. PubMed ID: 10594886 [TBL] [Abstract][Full Text] [Related]
5. Congenital hydrocephalus and eye abnormalities with severe developmental brain defects: Warburg's syndrome. Bordarier C; Aicardi J; Goutieres F Ann Neurol; 1984 Jul; 16(1):60-5. PubMed ID: 6431899 [TBL] [Abstract][Full Text] [Related]
7. [Walker-Warburg syndrome: experience at the Virgen de la Arrixaca Hospital]. Fernández Martínez MD; Rodríguez Sánchez F; Martínez-Lage Sánchez JF; Rodríguez Costa T; Puche Miras A; Casas Fernández C; Almagro Navarro MJ An Esp Pediatr; 1992 Mar; 36(3):213-7. PubMed ID: 1580433 [TBL] [Abstract][Full Text] [Related]
8. Three siblings with Walker-Warburg Syndrome. Bornemann A; Pfeiffer R; Beinder E; Wenkel H; Schlicker U; Meyermann R; Kirchner T Gen Diagn Pathol; 1996 May; 141(5-6):371-5. PubMed ID: 8780938 [TBL] [Abstract][Full Text] [Related]
9. Brief clinical report: HARD (+/- E) syndrome: report of a sixth family with support for autosomal-recessive inheritance. Aymé S; Mattei JF Am J Med Genet; 1983 Apr; 14(4):759-66. PubMed ID: 6405616 [TBL] [Abstract][Full Text] [Related]
10. Diagnostic criteria for Walker-Warburg syndrome. Dobyns WB; Pagon RA; Armstrong D; Curry CJ; Greenberg F; Grix A; Holmes LB; Laxova R; Michels VV; Robinow M Am J Med Genet; 1989 Feb; 32(2):195-210. PubMed ID: 2494887 [TBL] [Abstract][Full Text] [Related]
11. Disorder of cerebellar foliation in Walker's lissencephaly and neu-laxova syndrome. Lyon G; Raymond G; Mogami K; Gadisseux JF; Della Giustina E J Neuropathol Exp Neurol; 1993 Nov; 52(6):633-9. PubMed ID: 8229082 [TBL] [Abstract][Full Text] [Related]
12. [The Walker-Warburg syndrome. A new case]. Velin P; Dupont D; Lods F; Gambini L Pediatrie; 1987; 42(8):597-601. PubMed ID: 3129696 [TBL] [Abstract][Full Text] [Related]
13. Walker-Warburg syndrome: report of three affected sibs. Rodgers BL; Vanner LV; Pai GS; Sens MA Am J Med Genet; 1994 Jan; 49(2):198-201. PubMed ID: 8116667 [TBL] [Abstract][Full Text] [Related]
14. Cerebro-oculo-muscular syndrome: a variant of Fukuyama congenital cerebromuscular dystrophy. Dambska M; Wisniewski K; Sher J; Solish G Clin Neuropathol; 1982; 1(3):93-8. PubMed ID: 6820333 [TBL] [Abstract][Full Text] [Related]
15. Walker-Warburg syndrome with microtia and absent auditory canals. Gershoni-Baruch R; Mandel H; Miller B; Sujov P; Braun J Am J Med Genet; 1990 Sep; 37(1):87-91. PubMed ID: 2240049 [TBL] [Abstract][Full Text] [Related]
16. A familial syndrome of central nervous system and ocular malformations. Chemke J; Czernobilsky B; Mundel G; Barishak YR Clin Genet; 1975 Jan; 7(1):1-7. PubMed ID: 803883 [TBL] [Abstract][Full Text] [Related]
17. Cerebral abnormalities in the Neu-Laxova syndrome. Ostrovskaya TI; Lazjuk GI Am J Med Genet; 1988 Jul; 30(3):747-56. PubMed ID: 3055985 [TBL] [Abstract][Full Text] [Related]
18. Prenatal diagnosis of retinal detachment in Walker-Warburg syndrome. Farrell SA; Toi A; Leadman ML; Davidson RG; Caco C Am J Med Genet; 1987 Nov; 28(3):619-24. PubMed ID: 3122570 [TBL] [Abstract][Full Text] [Related]
19. The Walker-Warburg syndrome. De Wilde G; Hansens M; Govaert P Bull Soc Belge Ophtalmol; 1992; 243():129-38. PubMed ID: 1302142 [TBL] [Abstract][Full Text] [Related]