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 *

166 related articles for article (PubMed ID: 2896154)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. Ten families with fragile X syndrome: linkage relationships with four DNA probes from distal Xq.
    Buchanan JA; Buckton KE; Gosden CM; Newton MS; Clayton JF; Christie S; Hastie N
    Hum Genet; 1987 Jun; 76(2):165-72. PubMed ID: 3038730
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. Analysis of linkage relationships between genetic markers around the fragile X locus with special reference to the daughters of normal transmitting males.
    Winter RM; Pembrey ME
    Hum Genet; 1986 Sep; 74(1):93-7. PubMed ID: 3463533
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genetic mapping of the Xq27-q28 region: new RFLP markers useful for diagnostic applications in fragile-X and hemophilia-B families.
    Arveiler B; Oberlé I; Vincent A; Hofker MH; Pearson PL; Mandel JL
    Am J Hum Genet; 1988 Feb; 42(2):380-9. PubMed ID: 2893549
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. 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]  

  • 15. 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]  

  • 16. 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]  

  • 17. 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]  

  • 18. Improved DNA markers for efficient analysis of fragile X families.
    Heilig R; Oberlé I; Arveiler B; Hanauer A; Vidaud M; Mandel JL
    Am J Med Genet; 1988; 30(1-2):543-50. PubMed ID: 2902795
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 9.