BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

215 related articles for article (PubMed ID: 3674751)

  • 1. Genetic heterogeneity of X-linked mental retardation with fragile X. Association of tight linkage to factor IX and incomplete penetrance in males.
    Giannelli F; Morris AH; Garrett C; Daker M; Thurston C; Smith CA
    Ann Hum Genet; 1987 May; 51(2):107-24. PubMed ID: 3674751
    [TBL] [Abstract][Full Text] [Related]  

  • 2. DNA linkage studies in the fragile X syndrome suggest genetic heterogeneity.
    Brown WT; Gross AC; Chan CB; Jenkins EC
    Am J Med Genet; 1986; 23(1-2):643-64. PubMed ID: 3006490
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. The genetic distance between the coagulation factor IX gene and the locus for the fragile X syndrome: clinical implications.
    Forster-Gibson CJ; Mulligan LM; Partington MW; Simpson NE; Holden JJ; White BN
    J Neurogenet; 1985 Jun; 2(3):231-7. PubMed ID: 3860635
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genetic analysis of the fragile-X mental retardation syndrome with two flanking polymorphic DNA markers.
    Oberlé I; Heilig R; Moisan JP; Kloepfer C; Mattéi GM; Mattéi JF; Boué J; Froster-Iskenius U; Jacobs PA; Lathrop GM
    Proc Natl Acad Sci U S A; 1986 Feb; 83(4):1016-20. PubMed ID: 3006023
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Linkage analysis of X-linked mental retardation with and without fragile-X using factor IX gene probe.
    Choo KH; George D; Filby G; Halliday JL; Leversha M; Webb G; Danks DM
    Lancet; 1984 Aug; 2(8398):349. PubMed ID: 6146889
    [No Abstract]   [Full Text] [Related]  

  • 7. Linkage and recombination between fragile X-linked mental retardation and the factor IX gene.
    Warren ST; Glover TW; Davidson RL; Jagadeeswaran P
    Hum Genet; 1985; 69(1):44-6. PubMed ID: 3967889
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Further evidence for genetic heterogeneity in the fragile X syndrome.
    Brown WT; Jenkins EC; Gross AC; Chan CB; Krawczun MS; Duncan CJ; Sklower SL; Fisch GS
    Hum Genet; 1987 Apr; 75(4):311-21. PubMed ID: 2883105
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Linkage studies of X-linked mental retardation: high frequency of recombination in the telomeric region of the human X chromosome (fragile site/linkage/recombination/X chromosome).
    Davies KE; Mattei MG; Mattei JF; Veenema H; McGlade S; Harper K; Tommerup N; Nielsen KB; Mikkelsen M; Beighton P
    Hum Genet; 1985; 70(3):249-55. PubMed ID: 2991115
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The fragile X syndrome in a large family. III. Investigations on linkage of flanking DNA markers with the fragile site Xq27.
    Veenema H; Carpenter NJ; Bakker E; Hofker MH; Ward AM; Pearson PL
    J Med Genet; 1987 Jul; 24(7):413-21. PubMed ID: 2886667
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. Linkage heterogeneity and fragile X.
    Clayton JF; Gosden CM; Hastie ND; Evans HJ
    Hum Genet; 1988 Apr; 78(4):338-42. PubMed ID: 2896154
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Linkage analysis of families with fragile-X mental retardation, using a novel RFLP marker (DXS 304).
    Dahl N; Goonewardena P; Malmgren H; Gustavson KH; Holmgren G; Seemanova E; Annerén G; Flood A; Pettersson U
    Am J Hum Genet; 1989 Aug; 45(2):304-9. PubMed ID: 2569270
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. [Recombination between the fragile site Xq27 and the gene for coagulation factor IX].
    Landoulsi A; de Blois MC; Guérin P; Rethoré MO; Lejeune J; Lucotte G
    Ann Genet; 1985; 28(4):201-5. PubMed ID: 3879429
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Close linkage of fragile X-mental retardation syndrome to haemophilia B and transmission through a normal male.
    Camerino G; Mattei MG; Mattei JF; Jaye M; Mandel JL
    Nature; 1983 Dec 15-21; 306(5944):701-4. PubMed ID: 6689201
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Genetics and expression of the fragile X syndrome.
    Brown WT; Jenkins EC; Gross AC; Chan CB; Wisniewski K; Cohen IL; Miezejeski CM
    Ups J Med Sci Suppl; 1987; 44():137-54. PubMed ID: 2895523
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 11.