These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

148 related articles for article (PubMed ID: 3080875)

  • 1. Hunter syndrome: prenatal diagnosis in maternal serum.
    Zlotogora J; Bach G
    Am J Hum Genet; 1986 Feb; 38(2):253-60. PubMed ID: 3080875
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Iduronate sulfatase determination for the diagnosis of the Hunter syndrome and the detection of the carrier state.
    Neufeld EF; Liebaers I; Lim TW
    Adv Exp Med Biol; 1976; 68():253-60. PubMed ID: 820168
    [No Abstract]   [Full Text] [Related]  

  • 3. Iduronate sulfatase activity in serum, lymphocytes, and fibroblasts--simplified diagnosis of the Hunter syndrome.
    Liebaers I; Neufeld E
    Pediatr Res; 1976 Aug; 10(8):733-6. PubMed ID: 821034
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Heterozygote detection in Hunter syndrome.
    Zlotogora J; Bach G
    Am J Med Genet; 1984 Mar; 17(3):661-5. PubMed ID: 6424473
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Postnatal and prenatal diagnosis of mucopolysaccharidosis type II (Hunter syndrome)].
    Zhang WM; Shi HP; Li BT; Zhao SM; Qi QW; Sun NH; Huang SZ
    Zhonghua Er Ke Za Zhi; 2006 Sep; 44(9):644-7. PubMed ID: 17217652
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Hunter's syndrome: activity of iduronate sulfate sulfatase in the serum of pregnant heterozygotes.
    Zlotogora J; Bach G
    N Engl J Med; 1984 Aug; 311(5):331-2. PubMed ID: 6429538
    [No Abstract]   [Full Text] [Related]  

  • 7. 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; 112(1):107-12. PubMed ID: 6786801
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Prenatal diagnosis of Hunter syndrome using chorionic villi.
    Pannone N; Gatti R; Lombardo C; Di Natale P
    Prenat Diagn; 1986; 6(3):207-10. PubMed ID: 3088561
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Iduronate sulfatase in amniotic fluid: an aid in the prenatal diagnosis of the hunter syndrome.
    Liebaers I; Di Natale P; Neufeld EF
    J Pediatr; 1977 Mar; 90(3):423-5. PubMed ID: 402458
    [No Abstract]   [Full Text] [Related]  

  • 10. Detection of hunter heterozygotes by enzymatic analysis of hair roots.
    Nwokoro N; Neufeld EF
    Am J Hum Genet; 1979 Jan; 31(1):42-9. PubMed ID: 107796
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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; 30(6):575-82. PubMed ID: 106723
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Prenatal diagnosis of Hunter syndrome.
    Archer IM; Kingston HM; Harper PS
    Prenat Diagn; 1984; 4(3):195-200. PubMed ID: 6431402
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Feasibility of first trimester prenatal diagnosis of Hunter syndrome.
    Lykkelund C; Søndergaard F; Therkelsen AJ; Tønnesen T; Rasmussen V; Mikkelsen M; Güttler F; Nyland MH
    Lancet; 1983 Nov; 2(8359):1147. PubMed ID: 6138678
    [No Abstract]   [Full Text] [Related]  

  • 14. Prenatal diagnosis and carrier detection in mucopolysaccharidosis type II by mutation analysis. A 47,XXY male heterozygous for a missense point mutation.
    Bunge S; Steglich C; Lorenz P; Beck M; Xu S; Hopwood JJ; Gal A
    Prenat Diagn; 1994 Sep; 14(9):777-80. PubMed ID: 7845883
    [TBL] [Abstract][Full Text] [Related]  

  • 15. First-trimester diagnosis of Hunter syndrome: very low iduronate sulphatase activity in chorionic villi from a heterozygous female fetus.
    Cooper A; Thornley M; Wraith JE
    Prenat Diagn; 1991 Sep; 11(9):731-5. PubMed ID: 1820774
    [TBL] [Abstract][Full Text] [Related]  

  • 16. First trimester diagnosis of Hunter syndrome on chorionic villi.
    Kleijer WJ; van Diggelen OP; Janse HC; Galjaard H; Dumez Y; Boué J
    Lancet; 1984 Aug; 2(8400):472. PubMed ID: 6147543
    [No Abstract]   [Full Text] [Related]  

  • 17. Prenatal diagnosis of the Hunter syndrome and the introduction of a new fluorimetric enzyme assay.
    Keulemans JL; Sinigerska I; Garritsen VH; Huijmans JG; Voznyi YV; van Diggelen OP; Kleijer WJ
    Prenat Diagn; 2002 Nov; 22(11):1016-21. PubMed ID: 12424767
    [TBL] [Abstract][Full Text] [Related]  

  • 18. X-linked Hunter syndrome: the heterozygous phenotype in cell culture.
    Migeon BR; Sprenkle JA; Liebaers I; Scott JF; Neufeld EF
    Am J Hum Genet; 1977 Sep; 29(5):448-54. PubMed ID: 409283
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Prenatal diagnosis of Hunter syndrome using fetal plasma.
    Lissens W; Van Lierde M; Decaluwe J; Foulon W; Evrard P; Van Hoof F; Freund M; Liebaers I
    Prenat Diagn; 1988 Jan; 8(1):59-62. PubMed ID: 3125535
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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; 4(2):128-31. PubMed ID: 7981716
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.