BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

257 related articles for article (PubMed ID: 1677599)

  • 21. Mapping of DNA markers close to the fragile site on the human X chromosome at Xq27.3.
    Patterson M; Kenwrick S; Thibodeau S; Faulk K; Mattei MG; Mattei JF; Davies KE
    Nucleic Acids Res; 1987 Mar; 15(6):2639-51. PubMed ID: 2882476
    [TBL] [Abstract][Full Text] [Related]  

  • 22. DNA studies of X-linked mental retardation associated with a fragile site at Xq27.
    Davies KE
    Am J Med Genet; 1986; 23(1-2):633-42. PubMed ID: 3513572
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Pseudoautosomal linkage in schizophrenia.
    Curtis D; Kalsi G; Gurling HM
    Br J Psychiatry; 1994 Jul; 165(1):117-9. PubMed ID: 7953015
    [No Abstract]   [Full Text] [Related]  

  • 24. Manic-depressive illness and linkage reanalysis in the Xq27-Xq28 region of chromosome X.
    Mendelbaum K; Sevy S; Souery D; Papadimitriou GN; De Bruyn A; Raeymaekers P; Van Broeckhoven C; Mendlewicz J
    Neuropsychobiology; 1995; 31(2):58-63. PubMed ID: 7760986
    [TBL] [Abstract][Full Text] [Related]  

  • 25. New informative polymorphism at the DXS304 locus, a close distal marker for the fragile X locus.
    Rousseau F; Vincent A; Oberlé I; Mandel JL
    Hum Genet; 1990 Feb; 84(3):263-6. PubMed ID: 1968034
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Localisation of the gene for Hunter syndrome on the long arm of X chromosome.
    Upadhyaya M; Sarfarazi M; Bamforth JS; Thomas NS; Oberle I; Young I; Harper PS
    Hum Genet; 1986 Dec; 74(4):391-8. PubMed ID: 2878868
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Waisman syndrome, a human X-linked recessive basal ganglia disorder with mental retardation: localization to Xq27.3-qter.
    Gregg RG; Metzenberg AB; Hogan K; Sekhon G; Laxova R
    Genomics; 1991 Apr; 9(4):701-6. PubMed ID: 1674730
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Fragile X syndrome: genetic localisation by linkage mapping of two microsatellite repeats FRAXAC1 and FRAXAC2 which immediately flank the fragile site.
    Richards RI; Holman K; Kozman H; Kremer E; Lynch M; Pritchard M; Yu S; Mulley J; Sutherland GR
    J Med Genet; 1991 Dec; 28(12):818-23. PubMed ID: 1757956
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Strategies for linkage studies in schizophrenia.
    Mellon CD; Byerley WF
    Schizophr Res; 1989; 2(3):277-85. PubMed ID: 2577274
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Exclusion mapping of 12 X-linked disease loci and 10 DNA probes from the long arm of the X-chromosome.
    Yang HM; Lund T; Niebuhr E; Nørby S; Schwartz M; Shen L
    Clin Genet; 1990 Aug; 38(2):94-104. PubMed ID: 1976460
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Evidence against close linkage of unipolar affective illness to human chromosome 11p markers HRAS1 and INS and chromosome Xq marker DXS52.
    Neiswanger K; Slaugenhaupt SA; Hughes HB; Frank E; Frankel DR; McCarty MJ; Chakravarti A; Zubenko GS; Kupfer DJ; Kaplan BB
    Biol Psychiatry; 1990 Jul; 28(1):63-72. PubMed ID: 1973904
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Pulsed-field gradient-gel studies around the fragile site.
    Dobkin CS; Brown WT
    Am J Med Genet; 1988; 30(1-2):593-600. PubMed ID: 2902798
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Analysis of fragile X-mental retardation families using flanking polymorphic DNA probes.
    Goonewardena P; Gustavson KH; Holmgren G; Tolun A; Chotai J; Johnsen E; Pettersson U
    Clin Genet; 1986 Oct; 30(4):249-54. PubMed ID: 2878749
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Increase in the incidence of the fragile site Xq27 in prometaphases.
    Barbi G; Steinbach P
    Hum Genet; 1982; 61(1):82. PubMed ID: 6957373
    [No Abstract]   [Full Text] [Related]  

  • 35. Genetic mapping of two new DNA markers in Xq26-q28 relative to the fragile-X syndrome locus.
    Sood R; Mulligan LM; Poon R; White BN; Holden JJ
    Am J Hum Genet; 1990 Sep; 47(3):395-402. PubMed ID: 1975476
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Genes and psychosis: old wine in new bottles?
    Baron M
    Acta Psychiatr Scand; 1995 Aug; 92(2):81-6. PubMed ID: 7572264
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Myotubular myopathy in a girl with a deletion at Xq27-q28 and unbalanced X inactivation assigns the MTM1 gene to a 600-kb region.
    Dahl N; Hu LJ; Chery M; Fardeau M; Gilgenkrantz S; Nivelon-Chevallier A; Sidaner-Noisette I; Mugneret F; Gouyon JB; Gal A
    Am J Hum Genet; 1995 May; 56(5):1108-15. PubMed ID: 7726166
    [TBL] [Abstract][Full Text] [Related]  

  • 38. The identification of a third fragile site, FRAXF, in Xq27--q28 distal to both FRAXA and FRAXE.
    Hirst MC; Barnicoat A; Flynn G; Wang Q; Daker M; Buckle VJ; Davies KE; Bobrow M
    Hum Mol Genet; 1993 Feb; 2(2):197-200. PubMed ID: 8499907
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Linkage study of a susceptibility locus for schizophrenia in the pseudoautosomal region.
    Barr CL; Kennedy JL; Pakstis AJ; Castiglione CM; Kidd JR; Wetterberg L; Kidd KK
    Schizophr Bull; 1994; 20(2):277-86. PubMed ID: 8085132
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Genetic linkage heterogeneity in the fragile X syndrome.
    Brown WT; Gross AC; Chan CB; Jenkins EC
    Hum Genet; 1985; 71(1):11-8. PubMed ID: 2993154
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.