BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

111 related articles for article (PubMed ID: 1302002)

  • 1. Heritable unstable DNA sequences.
    Richards RI; Sutherland GR
    Nat Genet; 1992 Apr; 1(1):7-9. PubMed ID: 1302002
    [No Abstract]   [Full Text] [Related]  

  • 2. [Unstable DNA sequence and methylation in fragile X syndrome].
    Fu SD; Shen Y; Fan Y
    Zhonghua Yi Xue Za Zhi; 1994 Oct; 74(10):611-4, 646-7. PubMed ID: 7842338
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Evidence of founder chromosomes in fragile X syndrome.
    Richards RI; Holman K; Friend K; Kremer E; Hillen D; Staples A; Brown WT; Goonewardena P; Tarleton J; Schwartz C
    Nat Genet; 1992 Jul; 1(4):257-60. PubMed ID: 1302021
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Anticipation legitimized: unstable DNA to the rescue.
    Sutherland GR; Richards RI
    Am J Hum Genet; 1992 Jul; 51(1):7-9. PubMed ID: 1609807
    [No Abstract]   [Full Text] [Related]  

  • 5. Unstable triplet repeat sequences: a source of cancer mutations?
    Panzer S; Kuhl DP; Caskey CT
    Stem Cells; 1995 Mar; 13(2):146-57. PubMed ID: 7787780
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The unstable and methylatable mutations causing the fragile X syndrome.
    Rousseau F; Heitz D; Mandel JL
    Hum Mutat; 1992; 1(2):91-6. PubMed ID: 1301206
    [No Abstract]   [Full Text] [Related]  

  • 7. [Same mutation type behind several diseases. Repetition of trinucleotides is revealing].
    Anvret M; Edström L
    Lakartidningen; 1994 Oct; 91(43):3889. PubMed ID: 7967955
    [No Abstract]   [Full Text] [Related]  

  • 8. [Genetic studies in the neuropsychiatric disorders].
    Kondo I
    Tanpakushitsu Kakusan Koso; 1993 Feb; 38(3):327-34. PubMed ID: 8488267
    [No Abstract]   [Full Text] [Related]  

  • 9. Mutable mutation. Some genes cause diseases by growing and growing and..
    Rennie J
    Sci Am; 1992 May; 266(5):34. PubMed ID: 1566039
    [No Abstract]   [Full Text] [Related]  

  • 10. Questions of expansion.
    Mandel JL
    Nat Genet; 1993 May; 4(1):8-9. PubMed ID: 8513331
    [No Abstract]   [Full Text] [Related]  

  • 11. Trinucleotide repeat instability: when and where?
    Nelson DL; Warren ST
    Nat Genet; 1993 Jun; 4(2):107-8. PubMed ID: 8348143
    [No Abstract]   [Full Text] [Related]  

  • 12. Fragile X syndrome.
    Laxova R
    Adv Pediatr; 1994; 41():305-42. PubMed ID: 7992687
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Absence of chromosome fragility at 19q13.3 in patients with myotonic dystrophy.
    Jalal SM; Lindor NM; Michels VV; Buckley DD; Hoppe DA; Sarkar G; Dewald GW
    Am J Med Genet; 1993 Jun; 46(4):441-3. PubMed ID: 8357018
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Excess thymidine induces folate sensitive fragile sites.
    Sutherland GR; Baker E; Fratini A
    Am J Med Genet; 1985 Oct; 22(2):433-43. PubMed ID: 4050872
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Human genetics. The costs of instability.
    Davies KE
    Nature; 1992 Mar; 356(6364):15. PubMed ID: 1538769
    [No Abstract]   [Full Text] [Related]  

  • 16. [Fragile X syndrome].
    Yamagata T
    Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):509-12. PubMed ID: 9590115
    [No Abstract]   [Full Text] [Related]  

  • 17. [Last advances in Fragile X chromosome syndrome].
    Bañares VG
    Medicina (B Aires); 1995; 55(5 Pt 1):457-66. PubMed ID: 8728777
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A complex mutable polymorphism located within the fragile X gene.
    Zhong N; Dobkin C; Brown WT
    Nat Genet; 1993 Nov; 5(3):248-53. PubMed ID: 8275089
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Inability to induce fragile sites at CTG repeats in congenital myotonic dystrophy.
    Wenger SL; Giangreco CA; Tarleton J; Wessel HB
    Am J Med Genet; 1996 Dec; 66(1):60-3. PubMed ID: 8957513
    [TBL] [Abstract][Full Text] [Related]  

  • 20. FRAXAC2 instability.
    Mornet E; Chateau C; Taillandier A; Montagnon M; Simon-Bouy B; Serre JL; Boué A
    Nat Genet; 1994 Jun; 7(2):122-3. PubMed ID: 7920626
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.