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4. The systemic mucopolysaccharidoses. Ultrastructural and histochemical studies of conjunctiva and skin. Kenyon KR; Quigley HA; Hussels IE; Wyllie RG; Goldberg MF Am J Ophthalmol; 1972 Jun; 73(6):811-33. PubMed ID: 4260695 [No Abstract] [Full Text] [Related]
5. The systemic mucopolysaccharidoses. Spranger J Ergeb Inn Med Kinderheilkd; 1972; 32():165-265. PubMed ID: 4261654 [No Abstract] [Full Text] [Related]
6. Allelism, non-allelism and genetic compounds among the mucopolysaccharidoses: corrective factors in nosology, genetics and therapy. McKusick VA; Howell RR; Hussels IE; Neufeld EF; Stevenson RE Trans Assoc Am Physicians; 1972; 85():151-71. PubMed ID: 4267098 [No Abstract] [Full Text] [Related]
11. The detection of carriers and the problem of heterogeneity in genetic counseling. Porter IH Birth Defects Orig Artic Ser; 1970 May; 6(1):23-5. PubMed ID: 4257329 [No Abstract] [Full Text] [Related]
12. [Mucopolysaccharidoses. IV. Morphological contribution to the knowledge of mucopolysaccharidosis]. Magrini U; Scappaticci S Minerva Pediatr; 1972 Oct; 24(34):1609-28. PubMed ID: 4264143 [No Abstract] [Full Text] [Related]
13. [Diagnosis of hereditary mucopolysaccharidoses]. Onisawa J; Ri N; Nakamura R; Mizuno T; Suzuki Y Nihon Hifuka Gakkai Zasshi; 1972 Sep; 82(9):667-73. PubMed ID: 4265653 [No Abstract] [Full Text] [Related]
14. A distinct biochemical deficit in the Maroteaux-Lamy syndrome (mucopolysaccharidosis VI). Baron RW; Neufeld EF J Pediatr; 1972 Jan; 80(1):114-6. PubMed ID: 4259536 [No Abstract] [Full Text] [Related]
15. Vitamin A and mucopolysaccharidosis: a clinical and biochemical evaluation. Madsen JA; Linker A J Pediatr; 1969 Nov; 75(5):843-52. PubMed ID: 4243128 [No Abstract] [Full Text] [Related]
16. White blood cell cultures in genetic studies on the human mucopolysaccharidoses. Foley KM; Danes BS; Bearn AG Science; 1969 Apr; 164(3878):424-6. PubMed ID: 4180575 [TBL] [Abstract][Full Text] [Related]
18. Ultrastructure of the skin in the genetic mucopolysaccharidoses. Belcher RW Arch Pathol; 1972 Dec; 94(6):511-8. PubMed ID: 4263882 [No Abstract] [Full Text] [Related]
19. [Clinical and biochemical study of some hereditary metabolic diseases with nervous system lesions]. Gusev EI Zh Nevropatol Psikhiatr Im S S Korsakova; 1971; 71(10):1475-81. PubMed ID: 4257932 [No Abstract] [Full Text] [Related]
20. Abnormal arylsulphatase activities of fibroblasts cultured from patients with mucopolysaccharidosis and cystinosis. Furusho K; Vetrella M; Latta E Z Kinderheilkd; 1971; 110(4):324-31. PubMed ID: 4254863 [No Abstract] [Full Text] [Related] [Next] [New Search]