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    Results: 1 to 20 of 93

    1.

    "Idiopathic" mental retardation and new chromosomal abnormalities.

    Galasso C, Lo-Castro A, El-Malhany N, Curatolo P.

    Ital J Pediatr. 2010 Feb 14;36:17. Review.

    PMID:
    20152051
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    2.

    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.

    PMID:
    18047645
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    3.

    Diagnostic yield of various genetic approaches in patients with unexplained developmental delay or mental retardation.

    Rauch A, Hoyer J, Guth S, Zweier C, Kraus C, Becker C, Zenker M, Hüffmeier U, Thiel C, Rüschendorf F, Nürnberg P, Reis A, Trautmann U.

    Am J Med Genet A. 2006 Oct 1;140(19):2063-74.

    PMID:
    16917849
    [PubMed - indexed for MEDLINE]
    4.

    Subtelomeric chromosomal rearrangements detected in patients with idiopathic mental retardation and dysmorphic features.

    Caliskan MO, Karauzum SB, Mihci E, Tacoy S, Luleci G.

    Genet Couns. 2005;16(2):129-38.

    PMID:
    16080292
    [PubMed - indexed for MEDLINE]
    5.

    X linked mental retardation.

    Rejeb I, Ben Jemaa L, Chaabouni H.

    Tunis Med. 2009 May;87(5):311-8. Review.

    PMID:
    19927760
    [PubMed - indexed for MEDLINE]
    Free Article
    6.

    The discovery of microdeletion syndromes in the post-genomic era: review of the methodology and characterization of a new 1q41q42 microdeletion syndrome.

    Shaffer LG, Theisen A, Bejjani BA, Ballif BC, Aylsworth AS, Lim C, McDonald M, Ellison JW, Kostiner D, Saitta S, Shaikh T.

    Genet Med. 2007 Sep;9(9):607-16. Review.

    PMID:
    17873649
    [PubMed - indexed for MEDLINE]
    7.

    X-linked mental retardation: further lumping, splitting and emerging phenotypes.

    Kleefstra T, Hamel BC.

    Clin Genet. 2005 Jun;67(6):451-67. Review. Erratum in: Clin Genet. 2006 Feb;69(2):197.

    PMID:
    15857409
    [PubMed - indexed for MEDLINE]
    8.

    X-linked mental retardation.

    Lisik MZ, Sieron AL.

    Med Sci Monit. 2008 Nov;14(11):RA221-9. Review.

    PMID:
    18971887
    [PubMed - indexed for MEDLINE]
    9.

    [X-linked mental retardation--treatment scheme].

    Lisik MZ, Sieroń AL.

    Wiad Lek. 2008;61(4-6):146-53. Review. Polish.

    PMID:
    18939366
    [PubMed - indexed for MEDLINE]
    10.

    The use of genomic microarrays to study chromosomal abnormalities in mental retardation.

    Mao R, Pevsner J.

    Ment Retard Dev Disabil Res Rev. 2005;11(4):279-85. Review.

    PMID:
    16240409
    [PubMed - indexed for MEDLINE]
    11.

    Detection of chromosomal imbalances in children with idiopathic mental retardation by array based comparative genomic hybridisation (array-CGH).

    Schoumans J, Ruivenkamp C, Holmberg E, Kyllerman M, Anderlid BM, Nordenskjöld M.

    J Med Genet. 2005 Sep;42(9):699-705.

    PMID:
    16141005
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    12.

    X-linked mental retardation.

    Ropers HH, Hamel BC.

    Nat Rev Genet. 2005 Jan;6(1):46-57. Review.

    PMID:
    15630421
    [PubMed - indexed for MEDLINE]
    13.

    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 Jul-Sep;48(3):263-75.

    PMID:
    16179222
    [PubMed - indexed for MEDLINE]
    14.

    [Genetic mental retardation].

    Rodríguez-Revenga Bodi L, Madrigal-Bajo I, Milà-Racasens M.

    Rev Neurol. 2006 Oct 10;43 Suppl 1:S181-6. Review. Spanish.

    PMID:
    17061189
    [PubMed - indexed for MEDLINE]
    Free Article
    15.

    Final Report on Carcinogens Background Document for Formaldehyde.

    National Toxicology Program.

    Rep Carcinog Backgr Doc. 2010 Jan;(10-5981):i-512.

    PMID:
    20737003
    [PubMed - as supplied by publisher]
    16.

    Genomic microarrays in mental retardation: a practical workflow for diagnostic applications.

    Koolen DA, Pfundt R, de Leeuw N, Hehir-Kwa JY, Nillesen WM, Neefs I, Scheltinga I, Sistermans E, Smeets D, Brunner HG, van Kessel AG, Veltman JA, de Vries BB.

    Hum Mutat. 2009 Mar;30(3):283-92. Review.

    PMID:
    19085936
    [PubMed - indexed for MEDLINE]
    17.

    Chromosomal copy number changes in patients with non-syndromic X linked mental retardation detected by array CGH.

    Lugtenberg D, de Brouwer AP, Kleefstra T, Oudakker AR, Frints SG, Schrander-Stumpel CT, Fryns JP, Jensen LR, Chelly J, Moraine C, Turner G, Veltman JA, Hamel BC, de Vries BB, van Bokhoven H, Yntema HG.

    J Med Genet. 2006 Apr;43(4):362-70. Epub 2005 Sep 16. Erratum in: J Med Genet. 2008 Dec;45(12):832.

    PMID:
    16169931
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    18.

    Clinical utility of array CGH for the detection of chromosomal imbalances associated with mental retardation and multiple congenital anomalies.

    Edelmann L, Hirschhorn K.

    Ann N Y Acad Sci. 2009 Jan;1151:157-66. Review.

    PMID:
    19154522
    [PubMed - indexed for MEDLINE]
    19.

    Genome-wide screening using automated fluorescent genotyping to detect cryptic cytogenetic abnormalities in children with idiopathic syndromic mental retardation.

    Borck G, Rio M, Sanlaville D, Redon R, Molinari F, Bacq D, Raoul O, Cormier-Daire V, Lyonnet S, Amiel J, Le Merrer M, de Blois MC, Prieur M, Vekemans M, Carter NP, Munnich A, Colleaux L.

    Clin Genet. 2004 Aug;66(2):122-7.

    PMID:
    15253762
    [PubMed - indexed for MEDLINE]
    20.

    [Genetic causes of mental retardation].

    Rehder H, Fritz B.

    Wien Med Wochenschr. 2005 Jun;155(11-12):258-67. German.

    PMID:
    16035386
    [PubMed - indexed for MEDLINE]

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