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 *

234 related articles for article (PubMed ID: 8844067)

  • 1. Reverse mutations in the fragile X syndrome.
    Brown WT; Houck GE; Ding X; Zhong N; Nolin S; Glicksman A; Dobkin C; Jenkins EC
    Am J Med Genet; 1996 Aug; 64(2):287-92. PubMed ID: 8844067
    [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. Identification of small FRAXA premutations.
    Francis D; Burgess T; Mitchell J; Slater H
    Mol Diagn; 2000 Sep; 5(3):221-5. PubMed ID: 11070156
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The number of CGG repeats of the FMR1 locus in premutated and fully mutated heterozygotes and their offspring: implications for the origin of mosaicism.
    Mingroni-Netto RC; Haddad LA; Vianna-Morgante AM
    Am J Med Genet; 1996 Aug; 64(2):270-3. PubMed ID: 8844063
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Analysis of FMR1 (CGG)(n) alleles and DXS548-FRAXAC1 haplotypes in three European circumpolar populations: traces of genetic relationship with Asia.
    Larsen LA; Vuust J; Nystad M; Evseeva I; Van Ghelue M; Tranebjaerg L
    Eur J Hum Genet; 2001 Sep; 9(9):724-7. PubMed ID: 11571563
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Deletion in the FMR1 gene in a fragile-X male.
    Mannermaa A; Pulkkinen L; Kajanoja E; Ryynänen M; Saarikoski S
    Am J Med Genet; 1996 Aug; 64(2):293-5. PubMed ID: 8844068
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A deletion of 1.6 Kb proximal to the CGG repeat of the FMR1 gene causes fragile X-like psychological features.
    Wiegers AM; Curfs LM; Meijer H; Oostra B; Fryns JP
    Genet Couns; 1994; 5(4):377-80. PubMed ID: 7888141
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Molecular screening of fragile X (FRAXA) and FRAXE mental retardation syndromes in the Hellenic population of Greece and Cyprus: incidence, genetic variation, and stability.
    Patsalis PC; Sismani C; Hettinger JA; Boumba I; Georgiou I; Stylianidou G; Anastasiadou V; Koukoulli R; Pagoulatos G; Syrrou M
    Am J Med Genet; 1999 May; 84(3):184-90. PubMed ID: 10331587
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The effect of pre-mutation of X chromosome CGG trinucleotide repeats on brain anatomy.
    Moore CJ; Daly EM; Tassone F; Tysoe C; Schmitz N; Ng V; Chitnis X; McGuire P; Suckling J; Davies KE; Hagerman RJ; Hagerman PJ; Murphy KC; Murphy DG
    Brain; 2004 Dec; 127(Pt 12):2672-81. PubMed ID: 15483045
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Neuropsychological profiles of three sisters homozygous for the fragile X premutation.
    Mazzocco MM; Holden JJ
    Am J Med Genet; 1996 Aug; 64(2):323-8. PubMed ID: 8844074
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Fragile X syndrome and deletions in FMR1: new case and review of the literature.
    Hammond LS; Macias MM; Tarleton JC; Shashidhar Pai G
    Am J Med Genet; 1997 Nov; 72(4):430-4. PubMed ID: 9375726
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Analysis of FMR1 and flanking microsatellite markers in normal and fragile X chromosomes in Portugal: evidence for a "protector" haplotype.
    Peixoto A; dos Santos MR; Seruca R; Amorim A; Castedo S
    Eur J Hum Genet; 1998; 6(5):518-22. PubMed ID: 9801877
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Segregation of the fragile X mutation from a male with a full mutation: unusual somatic instability in the FMR-1 locus.
    Kambouris M; Snow K; Thibodeau S; Bluhm D; Green M; Feldman GL
    Am J Med Genet; 1996 Aug; 64(2):404-7. PubMed ID: 8844092
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Reduced FMR1 mRNA translation efficiency in fragile X patients with premutations.
    Primerano B; Tassone F; Hagerman RJ; Hagerman P; Amaldi F; Bagni C
    RNA; 2002 Dec; 8(12):1482-8. PubMed ID: 12515381
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Distribution of (CGG)n and FMR-1 associated microsatellite alleles in a normal Chilean population.
    Jara L; Aspillaga M; Avendaño I; Obreque V; Blanco R; Valenzuela CY
    Am J Med Genet; 1998 Jan; 75(3):277-82. PubMed ID: 9475597
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Haplotype and interspersion analysis of the FMR1 CGG repeat identifies two different mutational pathways for the origin of the fragile X syndrome.
    Eichler EE; Macpherson JN; Murray A; Jacobs PA; Chakravarti A; Nelson DL
    Hum Mol Genet; 1996 Mar; 5(3):319-30. PubMed ID: 8852655
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A fragile balance: FMR1 expression levels.
    Oostra BA; Willemsen R
    Hum Mol Genet; 2003 Oct; 12 Spec No 2():R249-57. PubMed ID: 12952862
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Parkinsonism, FXTAS, and FMR1 premutations.
    Toft M; Aasly J; Bisceglio G; Adler CH; Uitti RJ; Krygowska-Wajs A; Lynch T; Wszolek ZK; Farrer MJ
    Mov Disord; 2005 Feb; 20(2):230-3. PubMed ID: 15390127
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Fragile X-associated tremor/ataxia syndrome (FXTAS).
    Hagerman PJ; Hagerman RJ
    Ment Retard Dev Disabil Res Rev; 2004; 10(1):25-30. PubMed ID: 14994285
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.