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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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2006 | 1 |
2007 | 1 |
2008 | 2 |
2009 | 2 |
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2024 | 0 |
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The Odyssey of MeCP2 and parental imprinting.
Epigenetics. 2007 Jan-Mar;2(1):5-10. doi: 10.4161/epi.2.1.3697. Epub 2006 Dec 12.
Epigenetics. 2007.
PMID: 17965611
Free PMC article.
Review.
Neuron-specific impairment of inter-chromosomal pairing and transcription in a novel model of human 15q-duplication syndrome.
Meguro-Horike M, Yasui DH, Powell W, Schroeder DI, Oshimura M, Lasalle JM, Horike S.
Meguro-Horike M, et al.
Hum Mol Genet. 2011 Oct 1;20(19):3798-810. doi: 10.1093/hmg/ddr298. Epub 2011 Jul 1.
Hum Mol Genet. 2011.
PMID: 21725066
Free PMC article.
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A novel hypomorphic MECP2 point mutation is associated with a neuropsychiatric phenotype.
Adegbola AA, Gonzales ML, Chess A, LaSalle JM, Cox GF.
Adegbola AA, et al.
Hum Genet. 2009 Jan;124(6):615-23. doi: 10.1007/s00439-008-0585-6. Epub 2008 Nov 7.
Hum Genet. 2009.
PMID: 18989701
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Reciprocal co-regulation of EGR2 and MECP2 is disrupted in Rett syndrome and autism.
Swanberg SE, Nagarajan RP, Peddada S, Yasui DH, LaSalle JM.
Swanberg SE, et al.
Hum Mol Genet. 2009 Feb 1;18(3):525-34. doi: 10.1093/hmg/ddn380. Epub 2008 Nov 10.
Hum Mol Genet. 2009.
PMID: 19000991
Free PMC article.
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