BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

129 related articles for article (PubMed ID: 9034011)

  • 1. Cognitive, behavioral, and neuroanatomical assessment of two unrelated male children expressing FRAXE.
    Abrams MT; Doheny KF; Mazzocco MM; Knight SJ; Baumgardner TL; Freund LS; Davies KE; Reiss AL
    Am J Med Genet; 1997 Feb; 74(1):73-81. PubMed ID: 9034011
    [TBL] [Abstract][Full Text] [Related]  

  • 2. FMR2 expression in families with FRAXE mental retardation.
    Gécz J; Oostra BA; Hockey A; Carbonell P; Turner G; Haan EA; Sutherland GR; Mulley JC
    Hum Mol Genet; 1997 Mar; 6(3):435-41. PubMed ID: 9147647
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. Expansion and methylation status at FRAXE can be detected on EcoRI blots used for FRAXA diagnosis: analysis of four FRAXE families with mild mental retardation in males.
    Biancalana V; Taine L; Bouix JC; Finck S; Chauvin A; De Verneuil H; Knight SJ; Stoll C; Lacombe D; Mandel JL
    Am J Hum Genet; 1996 Oct; 59(4):847-54. PubMed ID: 8808600
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Screening for FMR1 and FMR2 mutations in 222 individuals from Spanish special schools: identification of a case of FRAXE-associated mental retardation.
    Milà M; Sànchez A; Badenas C; Brun C; Jiménez D; Villa MP; Castellví-Bel S; Estivill X
    Hum Genet; 1997 Oct; 100(5-6):503-7. PubMed ID: 9341861
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. FRAXE mutation in mentally retarded patients using the OxE18 probe.
    Mulatinho MV; Llerena JC; Pimentel MM
    Int J Mol Med; 2000 Jan; 5(1):67-9. PubMed ID: 10601577
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Implication of screening for FMR1 and FMR2 gene mutation in individuals with nonspecific mental retardation in Taiwan.
    Tzeng CC; Tzeng PY; Sun HS; Chen RM; Lin SJ
    Diagn Mol Pathol; 2000 Jun; 9(2):75-80. PubMed ID: 10850542
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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]  

  • 13. Molecular screening of FRAXA and FRAXE in Indian patients with unexplained mental retardation.
    Pandey UB; Phadke S; Mittal B
    Genet Test; 2002; 6(4):335-9. PubMed ID: 12537661
    [TBL] [Abstract][Full Text] [Related]  

  • 14. FRAXE mutation in a mentally retarded subject and in his phenotypically normal twin brother.
    Lo Nigro C; Faravelli F; Cavani S; Perroni L; Novello P; Vitali M; Bricarelli FD; Grasso M
    Eur J Hum Genet; 2000 Mar; 8(3):157-62. PubMed ID: 10780779
    [TBL] [Abstract][Full Text] [Related]  

  • 15. DNA diagnosis of FRAXA and FRAXE in Chinese children with neurodevelopmental disorders and fragile X syndrome.
    Chan SY; Wong V
    Clin Genet; 1998 Mar; 53(3):179-83. PubMed ID: 9630071
    [TBL] [Abstract][Full Text] [Related]  

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

  • 17. Mosaicism for FMR1 and FMR2 deletion: a new case.
    Fengler S; Fuchs S; König R; Arnemann J
    J Med Genet; 2002 Mar; 39(3):200-1. PubMed ID: 11897824
    [No Abstract]   [Full Text] [Related]  

  • 18. Prevalence of the fragile X syndrome in Yugoslav patients with non-specific mental retardation.
    Major T; Culjkovic B; Stojkovic O; Gucscekic M; Lakic A; Romac S
    J Neurogenet; 2003; 17(2-3):223-30. PubMed ID: 14668200
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molecular screening for fragile X syndrome among Indonesian children with developmental disability.
    Faradz SM; Buckley M; Lam-Po-Tang ; Leigh D; Holden JJ
    Am J Med Genet; 1999 Apr; 83(4):350-1. PubMed ID: 10208179
    [No Abstract]   [Full Text] [Related]  

  • 20. Fragile X syndrome with FMR1 and FMR2 deletion.
    Moore SJ; Strain L; Cole GF; Miedzybrodzka Z; Kelly KF; Dean JC
    J Med Genet; 1999 Jul; 36(7):565-6. PubMed ID: 10424820
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.