BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

161 related articles for article (PubMed ID: 1673306)

  • 21. Linkage analysis using multiple DNA polymorphic markers in normal families and in families with fragile X syndrome.
    Thibodeau SN; Dorkins HR; Faulk KR; Berry R; Smith AC; Hagerman R; King A; Davies KE
    Hum Genet; 1988 Jul; 79(3):219-27. PubMed ID: 3402993
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Linkage studies in a large fragile X family.
    Patterson M; Bell M; Kress W; Davies KE; Froster-Iskenius U
    Am J Hum Genet; 1988 Nov; 43(5):684-8. PubMed ID: 2903666
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Molecular characterization of a DNA probe, U6.2, located close to the fragile X locus.
    Pergolizzi R; Brown WT; Goonewardena P; Bhan R; Dobkin C; Dahl N; Pettersson U
    Am J Med Genet; 1991; 38(2-3):380-3. PubMed ID: 1673315
    [TBL] [Abstract][Full Text] [Related]  

  • 24. New polymorphisms at the DXS98 locus and confirmation of its location proximal to FRAXA by in situ hybridization.
    Schnur RE; Ledbetter SA; Ledbetter DH; Merry DE; Nussbaum RL
    Am J Hum Genet; 1989 Feb; 44(2):248-54. PubMed ID: 2563194
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Linkage homogeneity near the fragile X locus in normal and fragile X families.
    Suthers GK; Mulley JC; Voelckel MA; Dahl N; Väisänen ML; Steinbach P; Glass IA; Schwartz CE; van Oost BA; Thibodeau SN
    Genomics; 1991 Jul; 10(3):576-82. PubMed ID: 1889808
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Physical and genetic mapping of the CDR gene with particular reference to its position with respect to the FRAXA site.
    Siniscalco M; Oberlé I; Melis P; Alhadeff B; Murray J; Filippi G; Mattioni T; Chen YT; Furneaux H; Old LJ
    Am J Med Genet; 1991; 38(2-3):357-62. PubMed ID: 1708201
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. DNA studies of X-linked mental retardation associated with a fragile site at Xq27.3.
    Goonewardena P; Dahl N; Gustavson KH; Holmgren G; Pettersson U
    Ups J Med Sci Suppl; 1987; 44():155-64. PubMed ID: 2895524
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Prenatal diagnosis and carrier detection in fragile X.
    von Koskull H; Nordström AM; Salonen R; Peltonen L
    Am J Med Genet; 1992 Apr 15-May 1; 43(1-2):174-80. PubMed ID: 1605189
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Linkage between the fragile X and F9, DXS52 (St14), DXS98 (4D-8) and DXS105 (cX55.7).
    Mulley J; Turner G; Bain S; Sutherland GR
    Am J Med Genet; 1988; 30(1-2):567-80. PubMed ID: 2902797
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Efficient isolation of X chromosome-specific single-copy probes from a cosmid library of a human X/hamster hybrid-cell line: mapping of new probes close to the locus for X-linked mental retardation.
    Hofker MH; Bergen AA; Skraastad MI; Carpenter NJ; Veenema H; Connor JM; Bakker E; van Ommen GJ; Pearson PL
    Am J Hum Genet; 1987 Apr; 40(4):312-28. PubMed ID: 2883888
    [TBL] [Abstract][Full Text] [Related]  

  • 32. The polymorphic marker DXS304 is within 5 centimorgans of the fragile X locus.
    Vincent A; Dahl N; Oberlé I; Hanauer A; Mandel JL; Malmgren H; Pettersson U
    Genomics; 1989 Nov; 5(4):797-801. PubMed ID: 2574147
    [TBL] [Abstract][Full Text] [Related]  

  • 33. New distal marker closely linked to the fragile X locus.
    Hulsebos TJ; Oostra BA; Broersen S; Smits A; van Oost BA; Westerveld A
    Hum Genet; 1991 Jul; 87(3):369-72. PubMed ID: 1677926
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Multipoint genetic mapping of the Xq26-q28 region in families with fragile X mental retardation and in normal families reveals tight linkage of markers in q26-q27.
    Oberlé I; Camerino G; Wrogemann K; Arveiler B; Hanauer A; Raimondi E; Mandel JL
    Hum Genet; 1987 Sep; 77(1):60-5. PubMed ID: 3502701
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Multipoint linkage of 9 anonymous probes to HPRT, factor 9, and fragile X.
    Brown WT; Ye W; Gross AC; Chan CB; Dobkin CS; Jenkins EC
    Am J Med Genet; 1988; 30(1-2):551-66. PubMed ID: 2902796
    [TBL] [Abstract][Full Text] [Related]  

  • 36. A new DNA probe of potential use for diagnosis of the fragile-X syndrome.
    Lucotte G
    Ann Genet; 1990; 33(2):109-10. PubMed ID: 1978629
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Genetic mapping of DNA segments relative to the locus for the fragile-X syndrome at Xq27.3.
    Mulligan LM; Phillips MA; Forster-Gibson CJ; Beckett J; Partington MW; Simpson NE; Holden JJ; White BN
    Am J Hum Genet; 1985 May; 37(3):463-72. PubMed ID: 2988332
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Genetic and physical mapping of a novel region close to the fragile X site on the human X chromosome.
    Patterson MN; Bell MV; Bloomfield J; Flint T; Dorkins H; Thibodeau SN; Schaid D; Bren G; Schwartz CE; Wieringa B
    Genomics; 1989 May; 4(4):570-8. PubMed ID: 2744766
    [TBL] [Abstract][Full Text] [Related]  

  • 39. An assessment of the use of flanking DNA markers for fra(X) syndrome carrier detection and prenatal diagnosis.
    Forster-Gibson CJ; Mulligan LM; Simpson NE; White BN; Holden JJ
    Am J Med Genet; 1986; 23(1-2):665-83. PubMed ID: 3006491
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Physical mapping of probes proximal to the fragile X locus (FRAX) confirms the order F9-DXS105 (cX55.7)-DXS98 (4D8)-FRAXA.
    Sauer SM; Phelan MC; Richer CL; Schwartz CE
    Cytogenet Cell Genet; 1989; 50(2-3):172-3. PubMed ID: 2776486
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.