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 *

181 related articles for article (PubMed ID: 2878749)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. Study of a family with a fragile site of the X chromosome at Xq27-28 without mental retardation.
    Voelckel MA; Philip N; Piquet C; Pellissier MC; Oberlé I; Birg F; Mattei MG; Mattei JF
    Hum Genet; 1989 Mar; 81(4):353-7. PubMed ID: 2564838
    [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. 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]  

  • 10. 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]  

  • 11. Dissociation between mental retardation and fragile site expression in a family with fragile X-linked mental retardation.
    Voelckel MA; Mattei MG; N'Guyen C; Philip N; Birg F; Mattei JF
    Hum Genet; 1988 Dec; 80(4):375-8. PubMed ID: 2904402
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

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

  • 15. 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]  

  • 16. 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]  

  • 17. 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]  

  • 18. Linkage analysis using multiple Xq DNA polymorphisms in normal families, families with the fragile X syndrome, and other families with X linked conditions.
    Connor JM; Pirrit LA; Yates JR; Crossley JA; Imrie SJ; Colgan JM
    J Med Genet; 1987 Jan; 24(1):14-22. PubMed ID: 2879932
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Diagnostic molecular genetics of the fragile X.
    Sutherland GR; Mulley JC
    Clin Genet; 1990 Jan; 37(1):2-11. PubMed ID: 1967989
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.