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177 related items for PubMed ID: 8528670

  • 1. Presence of an IDS-related locus (IDS2) in Xq28 complicates the mutational analysis of Hunter syndrome.
    Bondeson ML, Malmgren H, Dahl N, Carlberg BM, Pettersson U.
    Eur J Hum Genet; 1995; 3(4):219-27. PubMed ID: 8528670
    [Abstract] [Full Text] [Related]

  • 2. Inversion of the IDS gene resulting from recombination with IDS-related sequences is a common cause of the Hunter syndrome.
    Bondeson ML, Dahl N, Malmgren H, Kleijer WJ, Tönnesen T, Carlberg BM, Pettersson U.
    Hum Mol Genet; 1995 Apr; 4(4):615-21. PubMed ID: 7633410
    [Abstract] [Full Text] [Related]

  • 3. Deletion of the Hunter gene and both DXS466 and DXS304 in a patient with mucopolysaccharidosis type II.
    Beck M, Steglich C, Zabel B, Dahl N, Schwinger E, Hopwood JJ, Gal A.
    Am J Med Genet; 1992 Sep 01; 44(1):100-3. PubMed ID: 1355630
    [Abstract] [Full Text] [Related]

  • 4. Evidence for an iduronate-sulfatase pseudogene near the functional Hunter syndrome gene in Xq27.3-q28.
    Rathmann M, Bunge S, Steglich C, Schwinger E, Gal A.
    Hum Genet; 1995 Jan 01; 95(1):34-8. PubMed ID: 7814022
    [Abstract] [Full Text] [Related]

  • 5. Two distinct deletions in the IDS gene and the gene W: a novel type of mutation associated with the Hunter syndrome.
    Karsten SL, Lagerstedt K, Carlberg BM, Kleijer WJ, Zaremba J, Van Diggelen OP, Czartoryska B, Pettersson U, Bondeson ML.
    Genomics; 1997 Jul 15; 43(2):123-9. PubMed ID: 9244428
    [Abstract] [Full Text] [Related]

  • 6. Molecular basis of iduronate-2-sulphatase gene mutations in patients with mucopolysaccharidosis type II (Hunter syndrome).
    Li P, Bellows AB, Thompson JN.
    J Med Genet; 1999 Jan 15; 36(1):21-7. PubMed ID: 9950361
    [Abstract] [Full Text] [Related]

  • 7. Sequence of the human iduronate 2-sulfatase (IDS) gene.
    Wilson PJ, Meaney CA, Hopwood JJ, Morris CP.
    Genomics; 1993 Sep 15; 17(3):773-5. PubMed ID: 8244397
    [Abstract] [Full Text] [Related]

  • 8. IDS gene-pseudogene exchange responsible for an intragenic deletion in a Hunter patient.
    Birot AM, Bouton O, Froissart R, Maire I, Bozon D.
    Hum Mutat; 1996 Sep 15; 8(1):44-50. PubMed ID: 8807335
    [Abstract] [Full Text] [Related]

  • 9. Molecular diagnosis of mucopolysaccharidosis type II (Hunter syndrome) by automated sequencing and computer-assisted interpretation: toward mutation mapping of the iduronate-2-sulfatase gene.
    Jonsson JJ, Aronovich EL, Braun SE, Whitley CB.
    Am J Hum Genet; 1995 Mar 15; 56(3):597-607. PubMed ID: 7887413
    [Abstract] [Full Text] [Related]

  • 10. Molecular analysis in patients with mucopolysaccharidosis type II suggests that DXS466 maps within the Hunter gene.
    Steglich C, Bunge S, Hulsebos T, Beck M, Brandt NJ, Schwinger E, Hopwood JJ, Gal A.
    Hum Genet; 1993 Sep 15; 92(2):179-82. PubMed ID: 8103756
    [Abstract] [Full Text] [Related]

  • 11. Frequent deletions at Xq28 indicate genetic heterogeneity in Hunter syndrome.
    Wilson PJ, Suthers GK, Callen DF, Baker E, Nelson PV, Cooper A, Wraith JE, Sutherland GR, Morris CP, Hopwood JJ.
    Hum Genet; 1991 Mar 15; 86(5):505-8. PubMed ID: 1901826
    [Abstract] [Full Text] [Related]

  • 12. DNA deletion confined to the iduronate-2-sulfatase promoter abolishes IDS gene expression.
    Timms KM, Huckett LE, Belmont JW, Shapira SK, Gibbs RA.
    Hum Mutat; 1998 Mar 15; 11(2):121-6. PubMed ID: 9482575
    [Abstract] [Full Text] [Related]

  • 13. Mutation analysis of the iduronate-2-sulfatase gene in patients with mucopolysaccharidosis type II (Hunter syndrome).
    Bunge S, Steglich C, Beck M, Rosenkranz W, Schwinger E, Hopwood JJ, Gal A.
    Hum Mol Genet; 1992 Aug 15; 1(5):335-9. PubMed ID: 1303211
    [Abstract] [Full Text] [Related]

  • 14. Identification of 9 novel IDS gene mutations in 19 unrelated Hunter syndrome (mucopolysaccharidosis Type II) patients. Mutations in brief no. 202. Online.
    Karsten SL, Voskoboeva E, Carlberg BM, Kleijer WJ, Tsnnesen T, Pettersson U, Bondeson ML.
    Hum Mutat; 1998 Aug 15; 12(6):433. PubMed ID: 10671065
    [Abstract] [Full Text] [Related]

  • 15. Double-strand breaks may initiate the inversion mutation causing the Hunter syndrome.
    Lagerstedt K, Karsten SL, Carlberg BM, Kleijer WJ, Tönnesen T, Pettersson U, Bondeson ML.
    Hum Mol Genet; 1997 Apr 15; 6(4):627-33. PubMed ID: 9097969
    [Abstract] [Full Text] [Related]

  • 16. 130 kb of DNA sequence reveals two new genes and a regional duplication distal to the human iduronate-2-sulfate sulfatase locus.
    Timms KM, Lu F, Shen Y, Pierson CA, Muzny DM, Gu Y, Nelson DL, Gibbs RA.
    Genome Res; 1995 Aug 15; 5(1):71-8. PubMed ID: 8717057
    [Abstract] [Full Text] [Related]

  • 17. A 38.8 kb deletion mutation of the iduronate-2-sulfatase gene in a patient with Hunter syndrome.
    Chou YY, Chao SC, Kuo PL, Lin SJ.
    J Formos Med Assoc; 2005 Apr 15; 104(4):273-5. PubMed ID: 15909065
    [Abstract] [Full Text] [Related]

  • 18. [A new mutation of iduronate-2-sulfatase gene from the patient with Hunter syndrome].
    Guo YB, Lin QD, Du CS.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Feb 15; 23(1):67-9. PubMed ID: 16456790
    [Abstract] [Full Text] [Related]

  • 19. Analysis of a 43.6 kb deletion in a patient with Hunter syndrome (MPSII): identification of a fusion transcript including sequences from the gene W and the IDS gene.
    Lagerstedt K, Carlberg BM, Karimi-Nejad R, Kleijer WJ, Bondeson ML.
    Hum Mutat; 2000 Feb 15; 15(4):324-31. PubMed ID: 10737977
    [Abstract] [Full Text] [Related]

  • 20. [Detection of a new mutation (T1140C)in a Chinese Guangdong patient with hunter syndrome].
    Guo YB, Du CS.
    Yi Chuan; 2006 May 15; 28(5):521-4. PubMed ID: 16735228
    [Abstract] [Full Text] [Related]

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