IDS gene-pseudogene exchange responsible for an intragenic deletion in a hunter patient
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference21 articles.
1. A 5-megabase familial deletion removes the IDS and FMR-1 genes in a male Hunter patient
2. Inversion of the IDS gene resulting from recombination with IDS-related sequences in a common cause of the Hunter syndrome
3. Presence of an IDS-Related Locus (IDS2) in Xq28 Complicates the Mutational Analysis of Hunter Syndrome
4. Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease
5. Isolation of a DNA probe of potential use for diagnosis of the fragile-X syndrome
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