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11. Syndromes with lissencephaly. II: Walker-Warburg and cerebro-oculo-muscular syndromes and a new syndrome with type II lissencephaly. Dobyns WB; Kirkpatrick JB; Hittner HM; Roberts RM; Kretzer FL Am J Med Genet; 1985 Sep; 22(1):157-95. PubMed ID: 3931474 [TBL] [Abstract][Full Text] [Related]
12. 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]
13. Inflammatory myopathy and Walker-Warburg syndrome: etiologic implications. Shevell MI; Rosenblatt B; Silver K Can J Neurol Sci; 1993 Aug; 20(3):227-9. PubMed ID: 8221388 [TBL] [Abstract][Full Text] [Related]
14. 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]
17. Muscle-eye-brain disease and Walker-Warburg syndrome: phenotype-genotype speculations. Commentary to Pihko's paper (pp. 57-61). Warburg M Brain Dev; 1995; 17(1):62-3. PubMed ID: 7762766 [No Abstract] [Full Text] [Related]
18. An unusual presentation of muscle-eye-brain disease: severe eye abnormalities with mild muscle and brain involvement. Demir E; Gucuyener K; Akturk A; Talim B; Konus O; Del Bo R; Ghezzi S; Comi GP Neuromuscul Disord; 2009 Oct; 19(10):692-5. PubMed ID: 19679478 [TBL] [Abstract][Full Text] [Related]