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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. 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]
4. [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]
5. 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]
6. 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]
7. 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]
8. 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]
9. 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]
10. 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]
11. 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]
12. Mucopolysaccharidosis type II (Hunter syndrome): characterization of the iduronate-2-sulphatase in MPS II skin fibroblasts. Petruschka L; Zschiesche M; Bielicki J; Seidlitz G; Machill G; Hopwood JJ; Herrmann FH J Inherit Metab Dis; 1994; 17(1):89-92. PubMed ID: 8051941 [No Abstract] [Full Text] [Related]
13. 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; 24(6):675-80. PubMed ID: 11768586 [TBL] [Abstract][Full Text] [Related]
14. 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]
15. Extension of the molecular analysis to the promoter region of the iduronate 2-sulfatase gene reveals genomic alterations in mucopolysaccharidosis type II patients with normal coding sequence. Brusius-Facchin AC; Abrahão L; Schwartz IV; Lourenço CM; Santos ES; Zanetti A; Tomanin R; Scarpa M; Giugliani R; Leistner-Segal S Gene; 2013 Sep; 526(2):150-4. PubMed ID: 23707223 [TBL] [Abstract][Full Text] [Related]
16. 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]