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 *

104 related articles for article (PubMed ID: 8844096)

  • 1. Trinucleotide repeat expansion in the FRAXE locus is not common among institutionalized individuals with non-specific developmental disabilities.
    Holden JJ; Julien-Inalsingh C; Chalifoux M; Wing M; Scott E; Fidler K; Swift I; Maidment B; Knight SJ; Davies KE; White BN
    Am J Med Genet; 1996 Aug; 64(2):420-3. PubMed ID: 8844096
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Trinucleotide repeats at the FRAXF locus: frequency and distribution in the general population.
    Holden JJ; Walker M; Chalifoux M; White BN
    Am J Med Genet; 1996 Aug; 64(2):424-7. PubMed ID: 8844097
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Expansion mutation frequency and CGG/GCC repeat polymorphism in FMR1 and FMR2 genes in an Indian population.
    Sharma D; Gupta M; Thelma BK
    Genet Epidemiol; 2001 Jan; 20(1):129-144. PubMed ID: 11119302
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A survey of FRAXE allele sizes in three populations.
    Zhong N; Ju W; Curley D; Wang D; Pietrofesa J; Wu G; Shen Y; Pang C; Poon P; Liu X; Gou S; Kajanoja E; Ryynänen M; Dobkin C; Brown WT
    Am J Med Genet; 1996 Aug; 64(2):415-9. PubMed ID: 8844095
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A new PCR assay useful for screening of FRAXE/FMR2 mental impairment among males.
    Santos CB; Costa Lima MA; Pimentel MM
    Hum Mutat; 2001 Aug; 18(2):157-62. PubMed ID: 11462240
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Lack of expansion of triplet repeats in the FMR1, FRAXE, and FRAXF loci in male multiplex families with autism and pervasive developmental disorders.
    Holden JJ; Wing M; Chalifoux M; Julien-Inalsingh C; Schutz C; Robinson P; Szatmari P; White BN
    Am J Med Genet; 1996 Aug; 64(2):399-403. PubMed ID: 8844091
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Trinucleotide CGG repeat in the FMR1 gene in Chinese mentally retarded patients.
    Pang CP; Poon PM; Chen QL; Lai KY; Yin CH; Zhao Z; Zhong N; Lau CH; Lam ST; Wong CK; Brown WT
    Am J Med Genet; 1999 May; 84(3):179-83. PubMed ID: 10331586
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The influence of expanded unmethylated alleles for FRAXA/FRAXE loci in the intellectual performance among Brazilian mentally impaired males.
    Barros Santos C; Gonçalves Pimentel MM
    Int J Mol Med; 2003 Sep; 12(3):385-9. PubMed ID: 12883656
    [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. Identification of FMR2, a novel gene associated with the FRAXE CCG repeat and CpG island.
    Gu Y; Shen Y; Gibbs RA; Nelson DL
    Nat Genet; 1996 May; 13(1):109-13. PubMed ID: 8673086
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Identification of the gene FMR2, associated with FRAXE mental retardation.
    Gecz J; Gedeon AK; Sutherland GR; Mulley JC
    Nat Genet; 1996 May; 13(1):105-8. PubMed ID: 8673085
    [TBL] [Abstract][Full Text] [Related]  

  • 12. FRAXE mutation analysis in three Spanish families.
    Carbonell P; López I; Gabarrón J; Bernabé MJ; Lucas JM; Guitart M; Gabau E; Glover G
    Am J Med Genet; 1996 Aug; 64(2):434-40. PubMed ID: 8844099
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [FRAXE mental retardation].
    Yamagata T
    Nihon Rinsho; 1999 Apr; 57(4):955-9. PubMed ID: 10222796
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Isolation of a GCC repeat showing expansion in FRAXF, a fragile site distal to FRAXA and FRAXE.
    Parrish JE; Oostra BA; Verkerk AJ; Richards CS; Reynolds J; Spikes AS; Shaffer LG; Nelson DL
    Nat Genet; 1994 Nov; 8(3):229-35. PubMed ID: 7874164
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genetic variation and intergenerational FMR1 CGG-repeat stability in 100 unrelated three-generation families from the normal population.
    Patsalis PC; Sismani C; Stylianou S; Ioannou P; Joseph G; Manoli P; Holden JJ; Hettinger JA
    Am J Med Genet; 1999 May; 84(3):217-20. PubMed ID: 10331595
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. FRAXA and FRAXE prevalence in patients with nonspecific mental retardation in the Hellenic population.
    Syrrou M; Georgiou I; Grigoriadou M; Petersen MB; Kitsiou S; Pagoulatos G; Patsalis PC
    Genet Epidemiol; 1998; 15(1):103-9. PubMed ID: 9523214
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Lack of FMR3 expression in a male with non-syndromic mental retardation and a microdeletion immediately distal to FRAXE CCG repeat.
    Santos-Rebouças CB; Abdalla CB; Fullston T; Campos M; Pimentel MM; Gécz J
    Neurosci Lett; 2006 Apr; 397(3):245-8. PubMed ID: 16469443
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 10 years' experience in fragile X testing among mentally retarded individuals in Greece: a molecular and epidemiological approach.
    Sofocleous C; Kitsiou S; Fryssira H; Kolialexi A; Kalaitzidaki M; Roma E; Tsangaris GT; Chistofidou C; Metaxotou C; Kanavakis E; Mavrou A
    In Vivo; 2008; 22(4):451-5. PubMed ID: 18712171
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Instability of the FMR2 trinucleotide repeat region associated with expanded FMR1 alleles.
    Brown TC; Tarleton JC; Go RC; Longshore JW; Descartes M
    Am J Med Genet; 1997 Dec; 73(4):447-55. PubMed ID: 9415473
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.