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Journal Abstract Search

294 related items for PubMed ID: 821034

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  • 4. Hunter's syndrome: activity of iduronate sulfate sulfatase in the serum of pregnant heterozygotes.
    Zlotogora J, Bach G.
    N Engl J Med; 1984 Aug 02; 311(5):331-2. PubMed ID: 6429538
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  • 5. Detection of Hunter syndrome (mucopolysaccharidosis type II) in Taiwanese: biochemical and linkage studies of the iduronate-2-sulfatase gene defects in MPS II patients and carriers.
    Lin SP, Chang JH, Lee-Chen GJ, Lin DS, Lin HY, Chuang CK.
    Clin Chim Acta; 2006 Jul 15; 369(1):29-34. PubMed ID: 16480701
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  • 6. Iduronate sulfatase analysis of hair roots for identification of Hunter syndrome heterozygotes.
    Yutaka T, Fluharty AL, Stevens RL, Kihara H.
    Am J Hum Genet; 1978 Nov 15; 30(6):575-82. PubMed ID: 106723
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  • 8. Hunter syndrome: presence of material cross-reacting with antibodies against iduronate sulfatase.
    Daniele A, Di Natale P.
    Hum Genet; 1987 Mar 15; 75(3):234-8. PubMed ID: 3104200
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  • 9. Hunter disease in a girl caused by R468Q mutation in the iduronate-2-sulfatase gene and skewed inactivation of the X chromosome carrying the normal allele.
    Sukegawa K, Song XQ, Masuno M, Fukao T, Shimozawa N, Fukuda S, Isogai K, Nishio H, Matsuo M, Tomatsu S, Kondo N, Orii T.
    Hum Mutat; 1997 Mar 15; 10(5):361-7. PubMed ID: 9375851
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  • 10. Carrier detection in Hunter syndrome.
    Archer IM, Young ID, Rees DW, Oladimeji A, Wusteman FS, Harper PS.
    Am J Med Genet; 1983 Sep 15; 16(1):61-9. PubMed ID: 6227239
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  • 11. alpha-L-iduronidase activity in leukocytes: diagnosis of homozygotes and heterozygotes of the Hurler syndrome.
    Omura K, Higami S, Tada K.
    Eur J Pediatr; 1976 May 04; 122(2):103-5. PubMed ID: 817912
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  • 13. Mutations of the iduronate-2-sulfatase (IDS) gene in patients with Hunter syndrome (mucopolysaccharidosis II).
    Schröder W, Wulff K, Wehnert M, Seidlitz G, Herrmann FH.
    Hum Mutat; 1994 May 04; 4(2):128-31. PubMed ID: 7981716
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  • 14. An improved assay for iduronate 2-sulphate sulphatase in serum and its use in the detection of carriers of the Hunter syndrome.
    Archer IM, Harper PS, Wusteman FS.
    Clin Chim Acta; 1981 Apr 27; 112(1):107-12. PubMed ID: 6786801
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  • 15. A fluorimetric enzyme assay for the diagnosis of MPS II (Hunter disease).
    Voznyi YV, Keulemans JL, van Diggelen OP.
    J Inherit Metab Dis; 2001 Nov 27; 24(6):675-80. PubMed ID: 11768586
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  • 16. Mucopolysaccharidosis type II (Hunter disease): identification and characterization of eight point mutations in the iduronate-2-sulfatase gene in Japanese patients.
    Sukegawa K, Tomatsu S, Fukao T, Iwata H, Song XQ, Yamada Y, Fukuda S, Isogai K, Orii T.
    Hum Mutat; 1995 Nov 27; 6(2):136-43. PubMed ID: 7581397
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