These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

154 related articles for article (PubMed ID: 2731932)

  • 1. Preliminary exclusion of an X-linked gene in Leber optic atrophy by linkage analysis.
    Chen JD; Cox I; Denton MJ
    Hum Genet; 1989 Jun; 82(3):203-7. PubMed ID: 2731932
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Reevaluation of the linkage of an optic atrophy susceptibility gene to X-chromosomal markers in Finnish families with Leber hereditary optic neuroretinopathy (LHON).
    Juvonen V; Vilkki J; Aula P; Nikoskelainen E; Savontaus ML
    Am J Hum Genet; 1993 Jul; 53(1):289-92. PubMed ID: 8317495
    [No Abstract]   [Full Text] [Related]  

  • 3. Evidence against an X-linked visual loss susceptibility locus in Leber hereditary optic neuropathy.
    Chalmers RM; Davis MB; Sweeney MG; Wood NW; Harding AE
    Am J Hum Genet; 1996 Jul; 59(1):103-8. PubMed ID: 8659512
    [TBL] [Abstract][Full Text] [Related]  

  • 4. X chromosome-linked and mitochondrial gene control of Leber hereditary optic neuropathy: evidence from segregation analysis for dependence on X chromosome inactivation.
    Bu XD; Rotter JI
    Proc Natl Acad Sci U S A; 1991 Sep; 88(18):8198-202. PubMed ID: 1896469
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Optic atrophy in Leber hereditary optic neuroretinopathy is probably determined by an X-chromosomal gene closely linked to DXS7.
    Vilkki J; Ott J; Savontaus ML; Aula P; Nikoskelainen EK
    Am J Hum Genet; 1991 Mar; 48(3):486-91. PubMed ID: 1998335
    [TBL] [Abstract][Full Text] [Related]  

  • 6. X-chromosomal gene in Leber hereditary optic neuroretinopathy.
    Chen JD; Denton MJ
    Am J Hum Genet; 1991 Sep; 49(3):692-3. PubMed ID: 1882847
    [No Abstract]   [Full Text] [Related]  

  • 7. Leber's hereditary optic neuroretinopathy and the X-chromosomal susceptibility factor: no linkage to DXs7.
    Carvalho MR; Müller B; Rötzer E; Berninger T; Kommerell G; Blankenagel A; Savontaus ML; Meitinger T; Lorenz B
    Hum Hered; 1992; 42(5):316-20. PubMed ID: 1360941
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Evidence against an X-linked locus close to DXS7 determining visual loss susceptibility in British and Italian families with Leber hereditary optic neuropathy.
    Sweeney MG; Davis MB; Lashwood A; Brockington M; Toscano A; Harding AE
    Am J Hum Genet; 1992 Oct; 51(4):741-8. PubMed ID: 1415219
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Segregation of mitochondrial genomes in a heteroplasmic lineage with Leber hereditary optic neuroretinopathy.
    Vilkki J; Savontaus ML; Nikoskelainen EK
    Am J Hum Genet; 1990 Jul; 47(1):95-100. PubMed ID: 1971999
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Leber hereditary optic neuropathy (LHON): a mitochondrial disease with unresolved complexities.
    Went LN
    Cytogenet Cell Genet; 1999; 86(2):153-6. PubMed ID: 10545708
    [No Abstract]   [Full Text] [Related]  

  • 11. Leber hereditary optic neuropathy: estimation of number of embryonic precursor cells and disease threshold in heterozygous affected females at the X-linked locus.
    Bu X; Rotter JI
    Clin Genet; 1992 Sep; 42(3):143-8. PubMed ID: 1395084
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The two locus control of Leber hereditary optic neuropathy and a high penetrance in Japanese pedigrees.
    Nakamura M; Fujiwara Y; Yamamoto M
    Hum Genet; 1993 May; 91(4):339-41. PubMed ID: 8500789
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The Leber hereditary optic neuropathy 14,484 mutation and X-linked adrenoleukodystrophy: a possible modifier of phenotypic expression?
    Gray RG; Green SH; Davies P; Alger S; Green A
    J Inherit Metab Dis; 1999 Aug; 22(6):760-1. PubMed ID: 10472539
    [No Abstract]   [Full Text] [Related]  

  • 14. Novel mutation in RP2 gene in two brothers with X-linked retinitis pigmentosa and mtDNA mutation of leber hereditary optic neuropathy who showed marked differences in clinical severity.
    Mashima Y; Saga M; Hiida Y; Imamura Y; Kudoh J; Shimizu N
    Am J Ophthalmol; 2000 Sep; 130(3):357-9. PubMed ID: 11020419
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Optic atrophy, hearing loss, and peripheral neuropathy.
    Hagemoser K; Weinstein J; Bresnick G; Nellis R; Kirkpatrick S; Pauli RM
    Am J Med Genet; 1989 May; 33(1):61-5. PubMed ID: 2665489
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Meiotic breakpoint mapping of a proposed X linked visual loss susceptibility locus in Leber's hereditary optic neuropathy.
    Handoko HY; Wirapati PJ; Sudoyo HA; Sitepu M; Marzuki S
    J Med Genet; 1998 Aug; 35(8):668-71. PubMed ID: 9719375
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Pedigree analysis in Leber hereditary optic neuropathy families with a pathogenic mtDNA mutation.
    Harding AE; Sweeney MG; Govan GG; Riordan-Eva P
    Am J Hum Genet; 1995 Jul; 57(1):77-86. PubMed ID: 7611298
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Restriction endonuclease analysis of leukocyte mitochondrial DNA in Leber's optic atrophy.
    Holt IJ; Miller DH; Harding AE
    J Neurol Neurosurg Psychiatry; 1988 Aug; 51(8):1075-7. PubMed ID: 2905730
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Leber's optic nerve atrophy; a mitochondrial hereditary disease].
    Oostra RJ; Bolhuis PA; Wijburg FA; Bleeker-Wagemakers EM
    Ned Tijdschr Geneeskd; 1995 Jul; 139(26):1327-31. PubMed ID: 7617050
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Dominant infantile optic nerve atrophy].
    Szedélyová L; Vaisová Z
    Cesk Oftalmol; 1989 Nov; 45(6):440-4. PubMed ID: 2605661
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.