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 *

163 related articles for article (PubMed ID: 3860635)

  • 1. 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]  

  • 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. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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]  

  • 13. [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]  

  • 14. 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]  

  • 15. 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]  

  • 16. New polymorphic DNA marker close to the fragile site FRAXA.
    Oostra BA; Hupkes PE; Perdon LF; van Bennekom CA; Bakker E; Halley DJ; Schmidt M; Du Sart D; Smits A; Wieringa B
    Genomics; 1990 Jan; 6(1):129-32. PubMed ID: 1968042
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Linkage relationships between DXS105, DXS98, and other polymorphic DNA markers flanking the fragile X locus.
    Carpenter NJ; Thibodeau SN; Brown WT
    Am J Med Genet; 1991; 38(2-3):349-53. PubMed ID: 1673310
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The fragile X syndrome.
    Brown WT
    Neurol Clin; 1989 Feb; 7(1):107-21. PubMed ID: 2646518
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. DNA linkage analysis of 26 families with fragile X syndrome.
    Carpenter NJ
    Am J Med Genet; 1991; 38(2-3):311-8. PubMed ID: 1673303
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.