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 *

185 related articles for article (PubMed ID: 1302021)

  • 1. 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]  

  • 2. Fragile X founder effects and new mutations in Finland.
    Zhong N; Kajanoja E; Smits B; Pietrofesa J; Curley D; Wang D; Ju W; Nolin S; Dobkin C; Ryynänen M; Brown WT
    Am J Med Genet; 1996 Jul; 64(1):226-33. PubMed ID: 8826481
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Evidence for high-risk haplotypes and (CGG)n expansion in fragile X syndrome in the Hellenic population of Greece and Cyprus.
    Syrrou M; Patsalis PC; Georgiou I; Hadjimarcou MI; Constantinou-Deltas CD; Pagoulatos G
    Am J Med Genet; 1996 Jul; 64(1):234-8. PubMed ID: 8826482
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Fragile X founder chromosome effects: linkage disequilibrium or microsatellite heterogeneity?
    Zhong N; Ye L; Dobkin C; Brown WT
    Am J Med Genet; 1994 Jul; 51(4):405-11. PubMed ID: 7943008
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Fragile X founder chromosomes in Italy: a few initial events and possible explanation for their heterogeneity.
    Chiurazzi P; Genuardi M; Kozak L; Giovannucci-Uzielli ML; Bussani C; Dagna-Bricarelli F; Grasso M; Perroni L; Sebastio G; Sperandeo MP; Oostra BA; Neri G
    Am J Med Genet; 1996 Jul; 64(1):209-15. PubMed ID: 8826478
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Pathology of unstable sequence of genome: fragile-X-syndrome].
    Beldjord C; Richard L
    C R Seances Soc Biol Fil; 1992; 186(4):363-70. PubMed ID: 1301224
    [TBL] [Abstract][Full Text] [Related]  

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

  • 9. Fragile X syndrome without CCG amplification has an FMR1 deletion.
    Gedeon AK; Baker E; Robinson H; Partington MW; Gross B; Manca A; Korn B; Poustka A; Yu S; Sutherland GR
    Nat Genet; 1992 Aug; 1(5):341-4. PubMed ID: 1302032
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Fragile X founder effect?
    Chakravarti A
    Nat Genet; 1992 Jul; 1(4):237-8. PubMed ID: 1302018
    [No Abstract]   [Full Text] [Related]  

  • 12. [Molecular and genetic features of fragile X syndrome].
    Jara L; Avendaño I; Aspillaga M; Blanco R
    Rev Med Chil; 1996 Jul; 124(7):865-72. PubMed ID: 9138377
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Unstable triplets and their mutational mechanism: size reduction of the CGG repeat vs. germline mosaicism in the fragile X syndrome.
    Chiurazzi P; Kozak L; Neri G
    Am J Med Genet; 1994 Jul; 51(4):517-21. PubMed ID: 7943033
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A point mutation in the FMR-1 gene associated with fragile X mental retardation.
    De Boulle K; Verkerk AJ; Reyniers E; Vits L; Hendrickx J; Van Roy B; Van den Bos F; de Graaff E; Oostra BA; Willems PJ
    Nat Genet; 1993 Jan; 3(1):31-5. PubMed ID: 8490650
    [TBL] [Abstract][Full Text] [Related]  

  • 15. High resolution genetic analysis suggests one ancestral predisposing haplotype for the origin of the myotonic dystrophy mutation.
    Neville CE; Mahadevan MS; Barceló JM; Korneluk RG
    Hum Mol Genet; 1994 Jan; 3(1):45-51. PubMed ID: 7909252
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Striking founder effect for the fragile X syndrome in Finland.
    Oudet C; von Koskull H; Nordström AM; Peippo M; Mandel JL
    Eur J Hum Genet; 1993; 1(3):181-9. PubMed ID: 8044645
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Fragile X syndrome and other dynamic mutation diseases.
    Sutherland GR; Richards RI
    Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():77-85. PubMed ID: 8629146
    [No Abstract]   [Full Text] [Related]  

  • 18. Fragile X mental retardation syndrome: from pathogenesis to diagnostic issues.
    Mandel JL; Biancalana V
    Growth Horm IGF Res; 2004 Jun; 14 Suppl A():S158-65. PubMed ID: 15135801
    [TBL] [Abstract][Full Text] [Related]  

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

  • 20. Direct detection of novel expanded trinucleotide repeats in the human genome.
    Schalling M; Hudson TJ; Buetow KH; Housman DE
    Nat Genet; 1993 Jun; 4(2):135-9. PubMed ID: 8348150
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.