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Journal Abstract Search

231 related items for PubMed ID: 8826443

  • 1. X chromosome inactivation and X-linked mental retardation.
    Willard HF.
    Am J Med Genet; 1996 Jul 12; 64(1):21-6. PubMed ID: 8826443
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  • 2. Systematic analysis of X-inactivation in 19XLMR families: extremely skewed profiles in carriers in three families.
    Raynaud M, Moizard MP, Dessay B, Briault S, Toutain A, Gendrot C, Ronce N, Moraine C.
    Eur J Hum Genet; 2000 Apr 12; 8(4):253-8. PubMed ID: 10854107
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  • 3. Skewed X inactivation in X-linked disorders.
    Van den Veyver IB.
    Semin Reprod Med; 2001 Jun 12; 19(2):183-91. PubMed ID: 11480916
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  • 8. X-linked genes and mental functioning.
    Skuse DH.
    Hum Mol Genet; 2005 Apr 15; 14 Spec No 1():R27-32. PubMed ID: 15809269
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  • 9. Determination of X-chromosome inactivation status using X-linked expressed polymorphisms identified by database searching.
    Kutsche R, Brown CJ.
    Genomics; 2000 Apr 01; 65(1):9-15. PubMed ID: 10777660
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  • 10. X-linked gene expression and X-chromosome inactivation: marsupials, mouse, and man compared.
    VandeBerg JL, Robinson ES, Samollow PB, Johnston PG.
    Isozymes Curr Top Biol Med Res; 1987 Apr 01; 15():225-53. PubMed ID: 3298156
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  • 11. Deletion mapping and X inactivation analysis of a non-specific mental retardation gene at Xp21.3-Xp22.11.
    Muroya K, Kinoshita E, Kamimaki T, Matsuo N, Yorifugi T, Ogata T.
    J Med Genet; 1999 Mar 01; 36(3):187-91. PubMed ID: 10204842
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  • 12. Genetic mapping of X-linked loci involved in skewing of X chromosome inactivation in the human.
    Naumova AK, Olien L, Bird LM, Smith M, Verner AE, Leppert M, Morgan K, Sapienza C.
    Eur J Hum Genet; 1998 Mar 01; 6(6):552-62. PubMed ID: 9887372
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  • 13. Inheritance of skewed X chromosome inactivation in a large family with an X-linked recessive deafness syndrome.
    Orstavik KH, Orstavik RE, Eiklid K, Tranebjaerg L.
    Am J Med Genet; 1996 Jul 12; 64(1):31-4. PubMed ID: 8826445
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  • 14. Paracentric inversion X(q21.2q24) associated with mental retardation in males and normal ovarian function in females.
    Abeliovich D, Dagan J, Kimchi-Sarfaty C, Zlotogora J.
    Am J Med Genet; 1995 Jan 30; 55(3):359-62. PubMed ID: 7726237
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  • 15. Nonspecific X-linked mental retardation II: the frequency in British Columbia.
    Herbst DS, Miller JR.
    Am J Med Genet; 1980 Jan 30; 7(4):461-9. PubMed ID: 7211956
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  • 17. Börjeson-Forssman-Lehmann syndrome in a woman with skewed X-chromosome inactivation.
    Kubota T, Oga S, Ohashi H, Iwamoto Y, Fukushima Y.
    Am J Med Genet; 1999 Nov 26; 87(3):258-61. PubMed ID: 10564881
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  • 18. Differential expression of alpha-fetoprotein genes on the inactive X chromosome in extraembryonic and somatic tissues of a transgenic mouse line.
    Krumlauf R, Chapman VM, Hammer RE, Brinster R, Tilghman SM.
    Nature; 1999 Nov 26; 319(6050):224-6. PubMed ID: 2418359
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  • 19. 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 Nov 26; 123(1-4):44-53. PubMed ID: 19287138
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  • 20. Assessment of X bends in patients with atypical X chromosome phenotypes.
    Munn CA, Wenger SL, Steele MW.
    Ann Genet; 1991 Nov 26; 34(2):120-4. PubMed ID: 1746882
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