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Journal Abstract Search

197 related items for PubMed ID: 9272741

  • 21. The gene for incontinentia pigmenti: failure of linkage studies using DNA probes to confirm cytogenetic localization.
    Harris A, Lankester S, Haan E, Beres J, Hulten M, Szollar J, Souttier L, Bobrow M.
    Clin Genet; 1988 Jul; 34(1):1-6. PubMed ID: 2900707
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  • 23. Familial idiopathic scoliosis: evidence of an X-linked susceptibility locus.
    Justice CM, Miller NH, Marosy B, Zhang J, Wilson AF.
    Spine (Phila Pa 1976); 2003 Mar 15; 28(6):589-94. PubMed ID: 12642767
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  • 24. Unstable pre-mutation may explain mosaic disease expression of incontinentia pigmenti in males.
    Traupe H, Vehring KH.
    Am J Med Genet; 1994 Feb 15; 49(4):397-8. PubMed ID: 8160732
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  • 25. Evidence for genetic heterogeneity in families with congenital motor nystagmus (CN).
    Oetting WS, Armstrong CM, Holleschau AM, DeWan AT, Summers GC.
    Ophthalmic Genet; 2000 Dec 15; 21(4):227-33. PubMed ID: 11135493
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  • 27. Diminished support for linkage between manic depressive illness and X-chromosome markers in three Israeli pedigrees.
    Baron M, Freimer NF, Risch N, Lerer B, Alexander JR, Straub RE, Asokan S, Das K, Peterson A, Amos J.
    Nat Genet; 1993 Jan 15; 3(1):49-55. PubMed ID: 8490654
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  • 28. Genetic mapping of X-linked ocular albinism: linkage analysis in a large Newfoundland kindred.
    Charles SJ, Green JS, Moore AT, Barton DE, Yates JR.
    Genomics; 1993 Apr 15; 16(1):259-61. PubMed ID: 8486368
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  • 29. De novo NEMO gene deletion (delta4-10)--a cause of incontinentia pigmenti in a female infant: a case report.
    Culić V, Gabrić D, Puizina-Ivić N, Rozman K, Peterlin B, Pavelić J.
    Coll Antropol; 2008 Dec 15; 32(4):1259-62. PubMed ID: 19149237
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  • 30. Evidence for a new locus for X-linked retinitis pigmentosa (RP23).
    Hardcastle AJ, Thiselton DL, Zito I, Ebenezer N, Mah TS, Gorin MB, Bhattacharya SS.
    Invest Ophthalmol Vis Sci; 2000 Jul 15; 41(8):2080-6. PubMed ID: 10892847
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  • 36. [Incontinentia pigmenti in a male patient].
    Burkhardt D, Schuffenhauer S, Peter RU, Walther JU, Ruzicka T.
    Hautarzt; 1993 Mar 15; 44(3):153-6. PubMed ID: 8463096
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  • 37. De novo mutation in three families with multigenerational incontinentia pigmenti.
    Scheuerle A, Lewis RA, Levy ML, Nelson DL.
    Am J Hum Genet; 1994 Dec 15; 55(6):1279-81. PubMed ID: 7977389
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  • 40. Evaluation of the norrie disease gene in a family with incontinentia pigmenti.
    Shastry BS, Trese MT.
    Ophthalmic Res; 2000 Dec 15; 32(4):181-4. PubMed ID: 10828739
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