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Journal Abstract Search

156 related items for PubMed ID: 2346203

  • 41. Leber's hereditary optic neuropathy: implications of the sex ratio for linkage studies in families with the 3460 ND1 mutation.
    Black GC, Craig IW, Oostra RJ, Norby S, Rosenberg T, Morten K, Laborde A, Poulton J.
    Eye (Lond); 1995; 9 ( Pt 4)():513-6. PubMed ID: 7498577
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  • 44. Risk of false-positive molecular genetic diagnosis of Leber's hereditary optic neuropathy.
    Mashima Y, Hiida Y, Saga M, Oguchi Y, Kudoh J, Shimizu N.
    Am J Ophthalmol; 1995 Feb; 119(2):245-6. PubMed ID: 7832241
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  • 49. Recent advances in Leber's hereditary optic neuroretinopathy.
    Nikoskelainen E, Vilkki J, Huoponen K, Savontaus ML.
    Eye (Lond); 1991 Feb; 5 ( Pt 3)():291-3. PubMed ID: 1955049
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  • 51. Screening for the two most frequent mutations in Leber's hereditary optic neuropathy by duplex PCR based on allele-specific amplification.
    Nørby S.
    Hum Mutat; 1993 Feb; 2(4):309-13. PubMed ID: 8401538
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  • 52. [Leber's hereditary optic neuropathy].
    Castier P, Francois P, Asseman R, Hemery B, Deleforge AM.
    Ophtalmologie; 1989 Feb; 3(3):199-202. PubMed ID: 2641110
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  • 53. Carbon monoxide poisoning as an epigenetic factor for Leber's hereditary optic neuropathy.
    Hwang JM, Park HW.
    Korean J Ophthalmol; 1996 Dec; 10(2):122-3. PubMed ID: 9055542
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