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Journal Abstract Search

249 related items for PubMed ID: 15857422

  • 1. Mutations found within exon 1 of MECP2 in Danish patients with Rett syndrome.
    Ravn K, Nielsen JB, Schwartz M.
    Clin Genet; 2005 Jun; 67(6):532-3. PubMed ID: 15857422
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  • 4. Mutations in exon 1 of MECP2B are not a common cause of X-linked mental retardation in males.
    Poirier K, Francis F, Hamel B, Moraine C, Fryns JP, Ropers HH, Chelly J, Bienvenu T.
    Eur J Hum Genet; 2005 May; 13(5):523-4. PubMed ID: 15770224
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  • 5. Methyl-CpG binding protein 2 gene (MECP2) variations in Japanese patients with Rett syndrome: pathological mutations and polymorphisms.
    Fukuda T, Yamashita Y, Nagamitsu S, Miyamoto K, Jin JJ, Ohmori I, Ohtsuka Y, Kuwajima K, Endo S, Iwai T, Yamagata H, Tabara Y, Miki T, Matsuishi T, Kondo I.
    Brain Dev; 2005 Apr; 27(3):211-7. PubMed ID: 15737703
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  • 6. Five novel frameshift mutations in exon 3 and 4 of the MECP2 gene identified in Rett patients: Consequences for the molecular diagnosis strategy.
    Bienvenu T, Souville I, Poirier K, Aquaviva C, Burglen L, Amiel J, Héron B, Kaminska A, Couvert P, Beldjord C, Chelly J.
    Hum Mutat; 2001 Sep; 18(3):251-2. PubMed ID: 11524737
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  • 7. MeCP2 in neurons: closing in on the causes of Rett syndrome.
    Caballero IM, Hendrich B.
    Hum Mol Genet; 2005 Apr 15; 14 Spec No 1():R19-26. PubMed ID: 15809268
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  • 8. [Mutational analysis of MECP2 gene in Rett syndrome].
    Pan H, Wang Y, Meng H, Bao X, Zhang Y, Shen Y, Wu X.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2002 Aug 15; 19(4):276-80. PubMed ID: 12170461
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  • 10. [How the methyl-CpG binding protein-related epigenetic disease turns on the genes that produce its symptoms].
    Horike S.
    Tanpakushitsu Kakusan Koso; 2005 Jul 15; 50(8):978-84. PubMed ID: 16001803
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  • 11. No mutations in the coding region of the Rett syndrome gene MECP2 in 59 autistic patients.
    Vourc'h P, Bienvenu T, Beldjord C, Chelly J, Barthélémy C, Müh JP, Andres C.
    Eur J Hum Genet; 2001 Jul 15; 9(7):556-8. PubMed ID: 11464249
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  • 12. [Clinical and molecular genetic findings in four girls with Rett syndrome].
    Deutscher K, Deutscher J, Bergmann L, Tefs K, Reichwald K, Schuster V.
    Klin Padiatr; 2002 Jul 15; 214(5):291-4. PubMed ID: 12235545
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  • 13. Gross rearrangements in the MECP2 gene in three patients with Rett syndrome: implications for routine diagnosis of Rett syndrome.
    Schollen E, Smeets E, Deflem E, Fryns JP, Matthijs G.
    Hum Mutat; 2003 Aug 15; 22(2):116-20. PubMed ID: 12872251
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  • 14. [Developmental disorder in girls due to Rett syndrome].
    Pruissen DM, Sinke RJ, Terhal PA, Beemer FA, Peters AC.
    Ned Tijdschr Geneeskd; 2003 Aug 09; 147(32):1560-3. PubMed ID: 12942847
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  • 15. Somatic mosaicism for a MECP2 mutation associated with classic Rett syndrome in a boy.
    Topçu M, Akyerli C, Sayi A, Törüner GA, Koçoğlu SR, Cimbiş M, Ozçelik T.
    Eur J Hum Genet; 2002 Jan 09; 10(1):77-81. PubMed ID: 11896459
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  • 16. Looping out links Rett syndrome with loss of imprinting error.
    Slow E.
    Clin Genet; 2005 May 09; 67(5):391-2. PubMed ID: 15811003
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  • 17. Histone modifications in Rett syndrome lymphocytes: a preliminary evaluation.
    Kaufmann WE, Jarrar MH, Wang JS, Lee YJ, Reddy S, Bibat G, Naidu S.
    Brain Dev; 2005 Aug 09; 27(5):331-9. PubMed ID: 16023547
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  • 18. DNA methylation and Rett syndrome.
    Kriaucionis S, Bird A.
    Hum Mol Genet; 2003 Oct 15; 12 Spec No 2():R221-7. PubMed ID: 12928486
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  • 19. [Mutational analysis of the MECP2 gene by direct sequencing in Hungarian patients with Rett syndrome].
    Kárteszi J, Hollódy K, Bene J, Morava E, Hadzsiev K, Czakó M, Melegh B, Kosztolányi G.
    Orv Hetil; 2004 Apr 25; 145(17):909-11. PubMed ID: 15170968
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  • 20. [Analysis of the most frequent mutations in girls with Rett syndrome].
    Rosipal R, Zeman J, Hadac J, Misovicová N, Nevsímalová S, Martásek P.
    Cas Lek Cesk; 2001 Aug 02; 140(15):473-6. PubMed ID: 11569169
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