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Journal Abstract Search

230 related items for PubMed ID: 26420639

  • 21. MECP2 duplication: possible cause of severe phenotype in females.
    Scott Schwoerer J, Laffin J, Haun J, Raca G, Friez MJ, Giampietro PF.
    Am J Med Genet A; 2014 Apr; 164A(4):1029-34. PubMed ID: 24458799
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  • 22. Different-sized duplications of Xq28, including MECP2, in three males with mental retardation, absent or delayed speech, and recurrent infections.
    Smyk M, Obersztyn E, Nowakowska B, Nawara M, Cheung SW, Mazurczak T, Stankiewicz P, Bocian E.
    Am J Med Genet B Neuropsychiatr Genet; 2008 Sep 05; 147B(6):799-806. PubMed ID: 18165974
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  • 25. [Diagnosis of MECP2 duplication syndrome with molecular genetic techniques].
    Yi Z, Wang S, Li L, Wu H, Ma Y, Qi Y, Pan H.
    Zhonghua Er Ke Za Zhi; 2014 Dec 05; 52(12):937-41. PubMed ID: 25619353
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  • 28. The clinical variability of the MECP2 duplication syndrome: description of two families with duplications excluding L1CAM and FLNA.
    Kirk EP, Malaty-Brevaud V, Martini N, Lacoste C, Levy N, Maclean K, Davies L, Philip N, Badens C.
    Clin Genet; 2009 Mar 05; 75(3):301-3. PubMed ID: 19018795
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  • 29. A sibship with duplication of Xq28 inherited from the mother; genomic characterization and clinical outcomes.
    Yon DK, Park JE, Kim SJ, Shim SH, Chae KY.
    BMC Med Genet; 2017 Mar 17; 18(1):30. PubMed ID: 28302064
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  • 34. Four unrelated patients with Lubs X-linked mental retardation syndrome and different Xq28 duplications.
    Bartsch O, Gebauer K, Lechno S, van Esch H, Froyen G, Bonin M, Seidel J, Thamm-Mücke B, Horn D, Klopocki E, Hertzberg C, Zechner U, Haaf T.
    Am J Med Genet A; 2010 Feb 17; 152A(2):305-12. PubMed ID: 20082459
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  • 37. Neurologic aspects of MECP2 gene duplication in male patients.
    Echenne B, Roubertie A, Lugtenberg D, Kleefstra T, Hamel BC, Van Bokhoven H, Lacombe D, Philippe C, Jonveaux P, de Brouwer AP.
    Pediatr Neurol; 2009 Sep 17; 41(3):187-91. PubMed ID: 19664534
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  • 39. MECP2 duplication syndrome in a Chinese family.
    Zhang Q, Zhao Y, Yang Y, Bao X.
    BMC Med Genet; 2015 Dec 16; 16():112. PubMed ID: 26672597
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