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Journal Abstract Search

767 related items for PubMed ID: 10447261

  • 1. A methylation PCR approach for detection of fragile X syndrome.
    Panagopoulos I, Lassen C, Kristoffersson U, Aman P.
    Hum Mutat; 1999; 14(1):71-9. PubMed ID: 10447261
    [Abstract] [Full Text] [Related]

  • 2. [Detection of FMR-1 gene expression by RT-PCR].
    Zheng L, Fan Y, Huang T, Zhu N, Shen Y, Wu G.
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1995 Dec; 17(6):407-11. PubMed ID: 9208564
    [Abstract] [Full Text] [Related]

  • 3. A novel PCR-based approach for the detection of the Huntington disease associated trinucleotide repeat expansion.
    Panagopoulos I, Lassen C, Kristoffersson U, Aman P.
    Hum Mutat; 1999 Dec; 13(3):232-6. PubMed ID: 10090478
    [Abstract] [Full Text] [Related]

  • 4. Molecular diagnosis of fragile X syndrome using methylation sensitive techniques in a cohort of patients with intellectual disability.
    Chaudhary AG, Hussein IR, Abuzenadah A, Gari M, Bassiouni R, Sogaty S, Lary S, Al-Quaiti M, Al Balwi M, Al Qahtani M.
    Pediatr Neurol; 2014 Apr; 50(4):368-76. PubMed ID: 24630283
    [Abstract] [Full Text] [Related]

  • 5. Multiplex methylation specific PCR analysis of fragile X syndrome: experience in Songklanagarind Hospital.
    Charalsawadi C, Sripo T, Limprasert P.
    J Med Assoc Thai; 2005 Aug; 88(8):1057-61. PubMed ID: 16404832
    [Abstract] [Full Text] [Related]

  • 6. Mosaicism in a fragile X male including a de novo deletion in the FMR1 gene.
    Petek E, Kroisel PM, Schuster M, Zierler H, Wagner K.
    Am J Med Genet; 1999 May 28; 84(3):229-32. PubMed ID: 10331598
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  • 8. 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 09; 64(2):293-5. PubMed ID: 8844068
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  • 12. Molecular-intelligence correlations in young fragile X males with a mild CGG repeat expansion in the FMR1 gene.
    Steyaert J, Borghgraef M, Legius E, Fryns JP.
    Am J Med Genet; 1996 Aug 09; 64(2):274-7. PubMed ID: 8844064
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  • 13. Mosaicism for full mutation and normal-sized allele of the FMR1 gene: a new case.
    Orrico A, Galli L, Dotti MT, Plewnia K, Censini S, Federico A.
    Am J Med Genet; 1998 Jul 24; 78(4):341-4. PubMed ID: 9714436
    [Abstract] [Full Text] [Related]

  • 14. 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 24; 18(2):157-62. PubMed ID: 11462240
    [Abstract] [Full Text] [Related]

  • 15. [A genetic and molecular study of 85 families affected with the fragile X syndrome].
    Milà Recasens M, Sánchez Díaz A, Glover López G, Castellví Bel S, Carbonell Meseguer P, Kruyer H, Ballesta Martínez F, Estivill Pallejà X.
    An Esp Pediatr; 1996 Mar 24; 44(3):250-6. PubMed ID: 8830601
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  • 16. Plastic microchip electrophoresis for genetic screening: the analysis of polymerase chain reactions products of fragile X (CGG)n alleles.
    Sung WC, Lee GB, Tzeng CC, Chen SH.
    Electrophoresis; 2001 Apr 24; 22(6):1188-93. PubMed ID: 11358146
    [Abstract] [Full Text] [Related]

  • 17. Methylation analysis of the fragile X syndrome by PCR.
    Das S, Kubota T, Song M, Daniel R, Berry-Kravis EM, Prior TW, Popovich B, Rosser L, Arinami T, Ledbetter DH.
    Genet Test; 2001 Apr 24; 1(3):151-5. PubMed ID: 10464640
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  • 18. Use of methylation sensitive polymerase chain reaction for detection of fragile X full mutation & carrier state in males.
    Karunasagar A, Pandit L, Kumar S, Karunasagar I, Karunasagar I.
    Indian J Med Res; 2005 Nov 24; 122(5):429-33. PubMed ID: 16456258
    [Abstract] [Full Text] [Related]

  • 19. A simple fragile X PCR assay with 7-deazaguanine-substituted DNA visualized by ethidium bromide.
    Cao J, Tarleton J, Barberio D, Davidow LS.
    Mol Cell Probes; 1994 Apr 24; 8(2):177-80. PubMed ID: 7935515
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  • 20. Genetic diversity at the FMR1 locus in Mexican population.
    Rosales-Reynoso MA, Mendoza-Carrera F, Troyo-Sanromán R, Medina C, Barros-Núñez P.
    Arch Med Res; 2005 Apr 24; 36(4):412-7. PubMed ID: 15950084
    [Abstract] [Full Text] [Related]

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