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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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1995 | 2 |
1997 | 1 |
1998 | 1 |
2024 | 0 |
PubMed for id: 3424
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Evidence for an iduronate-sulfatase pseudogene near the functional Hunter syndrome gene in Xq27.3-q28.
Hum Genet. 1995 Jan;95(1):34-8. doi: 10.1007/BF00225070.
Hum Genet. 1995.
PMID: 7814022
DNA variability and recombination rates at X-linked loci in humans.
Nachman MW, Bauer VL, Crowell SL, Aquadro CF.
Nachman MW, et al.
Genetics. 1998 Nov;150(3):1133-41. doi: 10.1093/genetics/150.3.1133.
Genetics. 1998.
PMID: 9799265
Free PMC article.
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Double-strand breaks may initiate the inversion mutation causing the Hunter syndrome.
Lagerstedt K, Karsten SL, Carlberg BM, Kleijer WJ, Tönnesen T, Pettersson U, Bondeson ML.
Lagerstedt K, et al.
Hum Mol Genet. 1997 Apr;6(4):627-33. doi: 10.1093/hmg/6.4.627.
Hum Mol Genet. 1997.
PMID: 9097969
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Inversion of the IDS gene resulting from recombination with IDS-related sequences is a common cause of the Hunter syndrome.
Bondeson ML, Dahl N, Malmgren H, Kleijer WJ, Tönnesen T, Carlberg BM, Pettersson U.
Bondeson ML, et al.
Hum Mol Genet. 1995 Apr;4(4):615-21. doi: 10.1093/hmg/4.4.615.
Hum Mol Genet. 1995.
PMID: 7633410
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