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Year | Number of Results |
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1994 | 1 |
1997 | 1 |
2001 | 1 |
2024 | 0 |
PubMed (cited) for id: 601491
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A translocation breakpoint cluster disrupts the newly defined 3' end of the SNURF-SNRPN transcription unit on chromosome 15.
Hum Mol Genet. 2001 Feb 1;10(3):201-10. doi: 10.1093/hmg/10.3.201.
Hum Mol Genet. 2001.
PMID: 11159938
An imprinted mouse transcript homologous to the human imprinted in Prader-Willi syndrome (IPW) gene.
Wevrick R, Francke U.
Wevrick R, et al.
Hum Mol Genet. 1997 Feb;6(2):325-32. doi: 10.1093/hmg/6.2.325.
Hum Mol Genet. 1997.
PMID: 9063754
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Identification of a novel paternally expressed gene in the Prader-Willi syndrome region.
Wevrick R, Kerns JA, Francke U.
Wevrick R, et al.
Hum Mol Genet. 1994 Oct;3(10):1877-82. doi: 10.1093/hmg/3.10.1877.
Hum Mol Genet. 1994.
PMID: 7849716
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