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6. Glyc-O-genetics of Walker-Warburg syndrome. van Reeuwijk J; Brunner HG; van Bokhoven H Clin Genet; 2005 Apr; 67(4):281-9. PubMed ID: 15733261 [TBL] [Abstract][Full Text] [Related]
7. Mutations of the POMT1 gene found in patients with Walker-Warburg syndrome lead to a defect of protein O-mannosylation. Akasaka-Manya K; Manya H; Endo T Biochem Biophys Res Commun; 2004 Dec; 325(1):75-9. PubMed ID: 15522202 [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]
10. Detection of an Alu insertion in the POMT1 gene from three French Walker Warburg syndrome families. Bouchet C; Vuillaumier-Barrot S; Gonzales M; Boukari S; Bizec CL; Fallet C; Delezoide AL; Moirot H; Laquerriere A; Encha-Razavi F; Durand G; Seta N Mol Genet Metab; 2007 Jan; 90(1):93-6. PubMed ID: 17079174 [TBL] [Abstract][Full Text] [Related]
11. Muscle-eye-brain disease and Walker-Warburg syndrome. Santavuori P; Pihko H; Sainio K; Lappi M; Somer H; Haltia M; Raitta C; Ketonen L; Leisti J Am J Med Genet; 1990 Jul; 36(3):371-4. PubMed ID: 2363444 [No Abstract] [Full Text] [Related]
12. A case associated with Walker Warburg syndrome phenotype and homozygous pericentric inversion 9: coincidental finding or aetiological factor? Zenker M; Dörr HG Acta Paediatr; 2000 Jun; 89(6):750-1. PubMed ID: 10914982 [No Abstract] [Full Text] [Related]
13. Agenesis of the corpus callosum and Dandy-Walker malformation associated with hemimegalencephaly in the sebaceous nevus syndrome. Dodge NN; Dobyns WB Am J Med Genet; 1995 Mar; 56(2):147-50. PubMed ID: 7625436 [TBL] [Abstract][Full Text] [Related]
14. The Walker-Warburg syndrome with cleft lip and palate. Pratap A; Agrawal A; Tiwari A; Lakshmi R; Rajbanshi S Singapore Med J; 2007 Feb; 48(2):e66-7. PubMed ID: 17304384 [TBL] [Abstract][Full Text] [Related]
18. Case report: two patients with oculocerebrocutaneous syndrome and terminal digital amputations. Asher NG; Olney AH; Schaefer GB Semin Pediatr Neurol; 2008 Dec; 15(4):221-3. PubMed ID: 19073332 [TBL] [Abstract][Full Text] [Related]
19. Association of holoprosencephaly and Down syndrome. Martinez-Frías ML Am J Med Genet; 1989 Mar; 32(3):435. PubMed ID: 2524971 [No Abstract] [Full Text] [Related]
20. The XK-aprosencephaly syndrome. Lurie IW; Nedzed MK; Lazjuk GI; Kirillova IA; Cherstvoy ED; Ostrovskaja TI; Shved IA Am J Med Genet; 1980; 7(2):231-4. PubMed ID: 7193413 [No Abstract] [Full Text] [Related] [Next] [New Search]