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Journal Abstract Search

133 related items for PubMed ID: 120803

  • 21. Mucopolysaccharidoses and mucolipidoses.
    Van Hoof F.
    J Clin Pathol Suppl (R Coll Pathol); 1974; 8():64-93. PubMed ID: 4220223
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  • 25. [Factors of phenotypic polymorphism and genetic consultation in thesaurismoses (review)].
    Aĭngorn ED, Timonina OV, Koroleva IA.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1980; 80(10):1564-71. PubMed ID: 6776723
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  • 27. Hurler-like disorders in infancy.
    Kelly TE.
    Clin Perinatol; 1976 Mar; 3(1):115-32. PubMed ID: 821689
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  • 28. [Hereditary connective tissue diseases. Mucopolysaccharidosis].
    Orii T.
    Nihon Rinsho; 1984 May; 42(5):1086-94. PubMed ID: 6433081
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  • 30. [Clinico-radiological findings in mucopolysaccharidosis. Description of 3 cases].
    Arciuli L.
    Pediatria (Napoli); 1976 Jun 30; 84(2):253-86. PubMed ID: 828253
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  • 31. Prenatal diagnosis of Maroteaux-Lamy syndrome.
    Van Dyke DL, Fluharty AL, Schafer IA, Shapiro LJ, Kihara H, Weiss L.
    Am J Med Genet; 1981 Jun 30; 8(2):235-42. PubMed ID: 6792921
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  • 32. Pseudoachondroplastic dysplasia (Maroteaux-Lamy): a critical analysis.
    Kozlowski K.
    Australas Radiol; 1976 Sep 30; 20(3):255-69. PubMed ID: 828853
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  • 33. Letter: Prenatal diagnosis of Maroteaux-Lamy syndrome.
    Kleijer WJ, Wolffers GM, Hoogeveen A, Niermeijer MF.
    Lancet; 1976 Jul 03; 2(7975):50. PubMed ID: 59120
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  • 34. Reclassification of previously reported cases of mucopolysaccharidosis type IS to mucopolysaccharidosis type VI.
    Constantopoulos G, Stowens DW, Barranger JA.
    Clin Chim Acta; 1982 Sep 01; 124(1):137-9. PubMed ID: 6812996
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  • 35. [Rare forms of joint diseases associated with arthritis].
    Nechvolodova OL, Iukina GP.
    Revmatologiia (Mosk); 1983 Sep 01; (4):61-4. PubMed ID: 6422531
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  • 36. An index case for the attenuated end of the mucopolysaccharidosis type VI clinical spectrum.
    Brooks DA, Gibson GJ, Karageorgos L, Hein LK, Robertson EF, Hopwood JJ.
    Mol Genet Metab; 2005 Jul 01; 85(3):236-8. PubMed ID: 15979036
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  • 37. Mucopolysaccharide storage disease in three families of cats with arylsulfatase B deficiency: leukocyte studies and carrier identification.
    Haskins ME, Jezyk PF, Patterson DF.
    Pediatr Res; 1979 Nov 01; 13(11):1203-10. PubMed ID: 229456
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  • 38. Deficiency of arylsulfatase B in 2 brothers aged 40 and 38 years (Maroteaux-Lamy syndrome, type B).
    Pilz H, von Figura K, Goebel HH.
    Ann Neurol; 1979 Oct 01; 6(4):315-25. PubMed ID: 122048
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