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Journal Abstract Search

111 related items for PubMed ID: 9006433

  • 1. Dominant optic atrophy, Kjer type. Linkage analysis and clinical features in a large British pedigree.
    Johnston RL, Burdon MA, Spalton DJ, Bryant SP, Behnam JT, Seller MJ.
    Arch Ophthalmol; 1997 Jan; 115(1):100-3. PubMed ID: 9006433
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  • 2. Clinical and genetic analysis of a family affected with dominant optic atrophy (OPA1).
    Brown J, Fingert JH, Taylor CM, Lake M, Sheffield VC, Stone EM.
    Arch Ophthalmol; 1997 Jan; 115(1):95-9. PubMed ID: 9006432
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  • 4. Genetic heterogeneity of dominant optic atrophy, Kjer type: Identification of a second locus on chromosome 18q12.2-12.3.
    Kerrison JB, Arnould VJ, Ferraz Sallum JM, Vagefi MR, Barmada MM, Li Y, Zhu D, Maumenee IH.
    Arch Ophthalmol; 1999 Jun; 117(6):805-10. PubMed ID: 10369594
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  • 7. Dominant optic atrophy mapped to chromosome 3q region. II. Clinical and epidemiological aspects.
    Kjer B, Eiberg H, Kjer P, Rosenberg T.
    Acta Ophthalmol Scand; 1996 Feb; 74(1):3-7. PubMed ID: 8689476
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  • 9. Linkage studies in dominant optic atrophy, Kjer type: possible evidence for heterogeneity.
    Seller MJ, Behnam JT, Lewis CM, Johnston RL, Burdon MA, Spalton DJ.
    J Med Genet; 1997 Dec; 34(12):967-72. PubMed ID: 9429135
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  • 11. Dominant optic atrophy (OPA1) mapped to chromosome 3q region. I. Linkage analysis.
    Eiberg H, Kjer B, Kjer P, Rosenberg T.
    Hum Mol Genet; 1994 Jun; 3(6):977-80. PubMed ID: 7951248
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  • 15. Electrophysiological findings in dominant optic atrophy (DOA) linking to the OPA1 locus on chromosome 3q 28-qter.
    Holder GE, Votruba M, Carter AC, Bhattacharya SS, Fitzke FW, Moore AT.
    Doc Ophthalmol; 1994 Jun; 95(3-4):217-28. PubMed ID: 10532406
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  • 19. Clinical heterogeneity in autosomal dominant optic atrophy in two 3q28-qter linked central Illinois families.
    Chen AS, Kovach MJ, Herman K, Avakian A, Frank W, Forrester S, Lin JP, Kimonis V.
    Genet Med; 2000 Jun; 2(5):283-9. PubMed ID: 11399209
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