Hunter syndrome: Gene deletions and rearrangements

This publication has 13 references indexed in Scilit:

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  American Journal of Medical Genetics, 1992
• Mutation analysis of the iduronate-2-sulfatase gene in patients with mucopolysaccharidosis type II (Hunter syndrome)
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• Detection of point mutations and a gross deletion in six Hunter Syndrome patients
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• Molecular analysis of patients with Hunter syndrome: implication of a region prone to structural alterations within the IDS gene
  Human Molecular Genetics, 1992
• Gene diagnosis and carrier detection in hunter syndrome by the iduronate‐2‐sulphatase cDNA probe
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• Intermediate form of mucopolysaccharidosis type II (Hunter disease): A C1327 to T substitution in the iduronate sulfatase gene
  Biochemical and Biophysical Research Communications, 1992
• The iduronate sulfatase gene: Isolation of a 1.2-Mb YAC contig spanning the entire gene and identification of heterogeneous deletions in patients with Hunter syndrome
  Genomics, 1992
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• New distal marker closely linked to the fragile X locus
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