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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2000 | 1 |
2003 | 2 |
2006 | 1 |
2024 | 0 |
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Page 1
Long-read sequence analysis of the MECP2 gene in Rett syndrome patients: correlation of disease severity with mutation type and location.
Hum Mol Genet. 2000 Apr 12;9(7):1119-29. doi: 10.1093/hmg/9.7.1119.
Hum Mol Genet. 2000.
PMID: 10767337
Developmental delay and the methyl binding genes.
Turner H, MacDonald F, Warburton S, Latif F, Webb T.
Turner H, et al.
J Med Genet. 2003 Feb;40(2):E13. doi: 10.1136/jmg.40.2.e13.
J Med Genet. 2003.
PMID: 12566531
Free PMC article.
No abstract available.
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Mutations and polymorphisms in the human methyl CpG-binding protein MECP2.
Miltenberger-Miltenyi G, Laccone F.
Miltenberger-Miltenyi G, et al.
Hum Mutat. 2003 Aug;22(2):107-15. doi: 10.1002/humu.10243.
Hum Mutat. 2003.
PMID: 12872250
Review.
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A new cohort of MECP2 mutation screening in unexplained mental retardation: careful re-evaluation is the best indicator for molecular diagnosis.
Donzel-Javouhey A, Thauvin-Robinet C, Cusin V, Madinier N, Manceau E, Dipanda D, Dulieu V, Mugneret F, Huet F, Teyssier JR, Faivre L.
Donzel-Javouhey A, et al.
Am J Med Genet A. 2006 Jul 15;140(14):1603-7. doi: 10.1002/ajmg.a.31314.
Am J Med Genet A. 2006.
PMID: 16763963
No abstract available.
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