Hunter Syndrome: Cloning of the Gene, Mutations and Carrier Detection

This publication has 44 references indexed in Scilit:

• Detection of point mutations and a gross deletion in six Hunter Syndrome patients
  Genomics, 1992
• Molecular analysis of patients with Hunter syndrome: implication of a region prone to structural alterations within the IDS gene
  Human Molecular Genetics, 1992
• Conference on gene therapy, Royal College of Physicians, London, 1 March 1990.
  Journal of Medical Genetics, 1990
• More precise localization of the gene for Hunter syndrome
  Genomics, 1990
• Further evidence localising the gene for Hunter's syndrome to the distal region of the X chromosome long arm.
  Journal of Medical Genetics, 1989
• Genetics of Hunter Syndrome: carrier detection, new mutations, segregation and linkage analysis
  Annals of Human Genetics, 1986
• Hunter's disease in a girl: association with X:5 chromosomal translocation disrupting the Hunter gene.
  Archives of Disease in Childhood, 1983
• The iduronate sulphatase activities of cells and tissue fluids from patients with Hunter syndrome and normal controls
  Journal of Inherited Metabolic Disease, 1983
• A clinical and genetic study of Hunter's syndrome. 1 Heterogeneity
  Journal of Medical Genetics, 1982
• Multiple forms of iduronate 2-sulphate sulphatase in human tissues and body fluids
  Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology, 1982