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4. The morquio A syndrome (mucopolysaccharidosis IVA) gene maps to 16q24.3. Baker E; Guo XH; Orsborn AM; Sutherland GR; Callen DF; Hopwood JJ; Morris CP Am J Hum Genet; 1993 Jan; 52(1):96-8. PubMed ID: 8434612 [TBL] [Abstract][Full Text] [Related]
5. Morquio B syndrome: a primary defect in beta-galactosidase. van der Horst GT; Kleijer WJ; Hoogeveen AT; Huijmans JG; Blom W; van Diggelen OP Am J Med Genet; 1983 Oct; 16(2):261-75. PubMed ID: 6418007 [TBL] [Abstract][Full Text] [Related]
6. A beta-galactosidase gene mutation identified in both Morquio B disease and infantile GM1 gangliosidosis. Suzuki Y; Oshima A Hum Genet; 1993 May; 91(4):407. PubMed ID: 8500799 [No Abstract] [Full Text] [Related]
8. Identification of a novel missense mutation in Brazilian patient with a severe form of mucopolysaccharidosis type IVA. Kubaski F; Brusius-Facchin AC; Palhares HM; Balarin MA; Viapiana-Camelier M; Guidobono R; Burin MG; Giugliani R; Leistner-Segal S Gene; 2013 Mar; 517(1):112-5. PubMed ID: 23313879 [TBL] [Abstract][Full Text] [Related]
9. Mucopolysaccharidoses type I and IVA: clinical features and consanguinity in Tunisia. Khedhiri S; Chkioua L; Bouzidi H; Dandana A; Ben Turkia H; Miled A; Laradi S Pathol Biol (Paris); 2009 Jul; 57(5):392-7. PubMed ID: 18584975 [TBL] [Abstract][Full Text] [Related]
10. Mutation analyses in 17 patients with deficiency in acid beta-galactosidase: three novel point mutations and high correlation of mutation W273L with Morquio disease type B. Paschke E; Milos I; Kreimer-Erlacher H; Hoefler G; Beck M; Hoeltzenbein M; Kleijer W; Levade T; Michelakakis H; Radeva B Hum Genet; 2001 Aug; 109(2):159-66. PubMed ID: 11511921 [TBL] [Abstract][Full Text] [Related]
11. [Late diagnosis of Morquio syndrome. Clinical histopathological findings in a rare mucopolysaccharidosis]. Gösele S; Dithmar S; Holz FG; Völcker HE Klin Monbl Augenheilkd; 2000 Aug; 217(2):114-7. PubMed ID: 11022666 [TBL] [Abstract][Full Text] [Related]