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Journal Abstract Search
503 related items for PubMed ID: 17217652
1. [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 [Abstract] [Full Text] [Related]
8. A novel fluorometric enzyme analysis method for Hunter syndrome using dried blood spots. Tolun AA, Graham C, Shi Q, Sista RS, Wang T, Eckhardt AE, Pamula VK, Millington DS, Bali DS. Mol Genet Metab; 2012 Mar; 105(3):519-21. PubMed ID: 22227323 [Abstract] [Full Text] [Related]
10. 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 [Abstract] [Full Text] [Related]
11. Prenatal diagnosis of Hunter syndrome using chorionic villi. Pannone N, Gatti R, Lombardo C, Di Natale P. Prenat Diagn; 1986 Sep; 6(3):207-10. PubMed ID: 3088561 [Abstract] [Full Text] [Related]
12. The iduronate sulphatase activities of cells and tissue fluids from patients with Hunter syndrome and normal controls. Dean MF. J Inherit Metab Dis; 1983 Sep; 6(3):108-11. PubMed ID: 6422140 [Abstract] [Full Text] [Related]