BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

98 related articles for article (PubMed ID: 6138678)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. First-trimester diagnosis of Hunter syndrome (MPS II).
    Besley GT; Broadhead DM; Ellis PM
    Prenat Diagn; 1992 Jan; 12(1):72-3. PubMed ID: 1557316
    [No 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. DNA and enzyme studies on chorionic villi for use in antenatal diagnosis.
    Upadhyaya M; Archer IM; Harper PS; Jasani B; Roberts A; Shaw DJ; Thomas NS; Williams H
    Clin Chim Acta; 1984 Jun; 140(1):39-46. PubMed ID: 6430598
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. Chorion biopsy for prenatal testing in Hunter's syndrome.
    Harper PS; Bamforth S; Rees D; Roberts A; Upadhyaya M
    Lancet; 1984 Oct; 2(8406):812-3. PubMed ID: 6148552
    [No Abstract]   [Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

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

  • 14. 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]  

  • 15. 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]  

  • 16. Prenatal diagnosis of hereditary tyrosinaemia type I by determination of fumarylacetoacetase in chorionic villus material.
    Kvittingen EA; Guibaud PP; Divry P; Mandon G; Rolland MO; Domenichini Y; Jakobs C; Christensen E
    Eur J Pediatr; 1986 Apr; 144(6):597-8. PubMed ID: 3709578
    [No Abstract]   [Full Text] [Related]  

  • 17. 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]  

  • 18. Biochemical diagnosis of Hunter syndrome on Epstein-Barr virus-transformed lymphoblastoid cell lines.
    Morabito E; Giambarrasi I; Rocchi M; Di Natale P
    Clin Chim Acta; 1989 May; 181(2):125-33. PubMed ID: 2567642
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Prenatal diagnosis of cystic fibrosis where single affected child has died: Guthrie spots and microvillar enzyme testing.
    McIntosh I; Strain L; Brock DJ
    Lancet; 1988 Nov; 2(8619):1085. PubMed ID: 2903315
    [No Abstract]   [Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 5.