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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1992 | 2 |
1993 | 1 |
2024 | 0 |
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Molecular diagnosis of the Prader-Willi and Angelman syndromes by detection of parent-of-origin specific DNA methylation in 15q11-13.
Hum Genet. 1992 Nov;90(3):313-5. doi: 10.1007/BF00220089.
Hum Genet. 1992.
PMID: 1487250
Difference in methylation patterns within the D15S9 region of chromosome 15q11-13 in first cousins with Angelman syndrome and Prader-Willi syndrome.
Clayton-Smith J, Driscoll DJ, Waters MF, Webb T, Andrews T, Malcolm S, Pembrey ME, Nicholls RD.
Clayton-Smith J, et al.
Am J Med Genet. 1993 Oct 1;47(5):683-6. doi: 10.1002/ajmg.1320470519.
Am J Med Genet. 1993.
PMID: 8266996
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A DNA methylation imprint, determined by the sex of the parent, distinguishes the Angelman and Prader-Willi syndromes.
Driscoll DJ, Waters MF, Williams CA, Zori RT, Glenn CC, Avidano KM, Nicholls RD.
Driscoll DJ, et al.
Genomics. 1992 Aug;13(4):917-24. doi: 10.1016/0888-7543(92)90001-9.
Genomics. 1992.
PMID: 1505981
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