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Journal Abstract Search

274 related items for PubMed ID: 17980689

  • 1. Screening of 20 patients with X-linked mental retardation using chromosome X-specific array-MAPH.
    Kousoulidou L, Parkel S, Zilina O, Palta P, Puusepp H, Remm M, Turner G, Boyle J, van Bokhoven H, de Brouwer A, Van Esch H, Froyen G, Ropers HH, Chelly J, Moraine C, Gecz J, Kurg A, Patsalis PC.
    Eur J Med Genet; 2007; 50(6):399-410. PubMed ID: 17980689
    [Abstract] [Full Text] [Related]

  • 2. X chromosome array-CGH for the identification of novel X-linked mental retardation genes.
    Bauters M, Van Esch H, Marynen P, Froyen G.
    Eur J Med Genet; 2005; 48(3):263-75. PubMed ID: 16179222
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  • 3. Detection of genomic copy number changes in patients with idiopathic mental retardation by high-resolution X-array-CGH: important role for increased gene dosage of XLMR genes.
    Froyen G, Van Esch H, Bauters M, Hollanders K, Frints SG, Vermeesch JR, Devriendt K, Fryns JP, Marynen P.
    Hum Mutat; 2007 Oct; 28(10):1034-42. PubMed ID: 17546640
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  • 4. Detection of small genomic imbalances using microarray-based multiplex amplifiable probe hybridization.
    Patsalis PC, Kousoulidou L, Männik K, Sismani C, Zilina O, Parkel S, Puusepp H, Tõnisson N, Palta P, Remm M, Kurg A.
    Eur J Hum Genet; 2007 Feb; 15(2):162-72. PubMed ID: 17119536
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  • 5. Copy-number variations on the X chromosome in Japanese patients with mental retardation detected by array-based comparative genomic hybridization analysis.
    Honda S, Hayashi S, Imoto I, Toyama J, Okazawa H, Nakagawa E, Goto Y, Inazawa J.
    J Hum Genet; 2010 Sep; 55(9):590-9. PubMed ID: 20613765
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  • 9. X-linked mental retardation, short stature, microcephaly and hypogonadism maps to Xp22.1-p21.3 in a Belgian family.
    Van Esch H, Zanni G, Holvoet M, Borghgraef M, Chelly J, Fryns JP, Devriendt K.
    Eur J Med Genet; 2005 Sep; 48(2):145-52. PubMed ID: 16053905
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  • 12. Detection and validation of copy number variation in X-linked mental retardation.
    Bauters M, Weuts A, Vandewalle J, Nevelsteen J, Marynen P, Van Esch H, Froyen G.
    Cytogenet Genome Res; 2008 Sep; 123(1-4):44-53. PubMed ID: 19287138
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  • 14. X-chromosome tiling path array detection of copy number variants in patients with chromosome X-linked mental retardation.
    Madrigal I, Rodríguez-Revenga L, Armengol L, González E, Rodriguez B, Badenas C, Sánchez A, Martínez F, Guitart M, Fernández I, Arranz JA, Tejada M, Pérez-Jurado LA, Estivill X, Milà M.
    BMC Genomics; 2007 Nov 29; 8():443. PubMed ID: 18047645
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  • 16. Mutation screening of the Aristaless-related homeobox (ARX) gene in Thai pediatric patients with delayed development: first report from Thailand.
    Rujirabanjerd S, Tongsippunyoo K, Sripo T, Limprasert P.
    Eur J Med Genet; 2007 Nov 29; 50(5):346-54. PubMed ID: 17613295
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  • 18. The genetics of mental retardation.
    Raymond FL, Tarpey P.
    Hum Mol Genet; 2006 Oct 15; 15 Spec No 2():R110-6. PubMed ID: 16987873
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  • 19. Array-MAPH: a methodology for the detection of locus copy-number changes in complex genomes.
    Kousoulidou L, Männik K, Sismani C, Zilina O, Parkel S, Puusepp H, Tõnisson N, Palta P, Remm M, Kurg A, Patsalis PC.
    Nat Protoc; 2008 Oct 15; 3(5):849-65. PubMed ID: 18451793
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