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 *

152 related articles for article (PubMed ID: 20217280)

  • 1. A unified rapid PCR method for detection of normal and expanded trinucleotide alleles of CAG repeats in huntington chorea and CGG repeats in fragile X syndrome.
    Todorov T; Todorova A; Georgieva B; Mitev V
    Mol Biotechnol; 2010 Jun; 45(2):150-4. PubMed ID: 20217280
    [TBL] [Abstract][Full Text] [Related]  

  • 2. PCR approach for detection of Fragile X syndrome and Huntington disease based on modified DNA: limits and utility.
    Rosales-Reynoso MA; Vilatela EA; Ojeda RM; Arce-Rivas A; Sandoval L; Troyo-Sanromán R; Barros-Núñez P
    Genet Test; 2007; 11(2):153-9. PubMed ID: 17627386
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 4. High-throughput analysis of fragile X (CGG)n alleles in the normal and premutation range by PCR amplification and automated capillary electrophoresis.
    Larsen LA; Grønskov K; Nørgaard-Pedersen B; Brøndum-Nielsen K; Hasholt L; Vuust J
    Hum Genet; 1997 Oct; 100(5-6):564-8. PubMed ID: 9341871
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Computer simulation of expansions of DNA triplet repeats in the fragile X syndrome and Huntington's disease.
    Bat O; Kimmel M; Axelrod DE
    J Theor Biol; 1997 Sep; 188(1):53-67. PubMed ID: 9299309
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Molecular diagnosis of fragile X syndrome and distribution of CGG repeats in the FMR-1 gene in Taiwanese.
    Wang YC; Li C; Lin ML; Lin WH; Li SY
    J Formos Med Assoc; 2000 May; 99(5):402-7. PubMed ID: 10870330
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Simple molecular diagnostic method for fragile X syndrome in Egyptian patients: pilot study.
    Meguid NA; Ismail MF; El-Mahdy RS; Barakat MA; El-Awady MK
    Acta Biochim Pol; 2014; 61(2):259-63. PubMed ID: 24936518
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Improved fluorescent PCR-based assay for sizing CGG repeats at the FRAXA locus.
    Houdayer C; Lemonnier A; Gerard M; Chauve C; Tredano M; de Villemeur TB; Aymard P; Bonnefont JP; Feldmann D
    Clin Chem Lab Med; 1999 Apr; 37(4):397-402. PubMed ID: 10369109
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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; 22(6):1188-93. PubMed ID: 11358146
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Frequency of FMR1 premutations in a consecutive newborn population by PCR screening of Guthrie blood spots.
    Dawson AJ; Chodirker BN; Chudley AE
    Biochem Mol Med; 1995 Oct; 56(1):63-9. PubMed ID: 8593539
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Analysis of CGG repeat instability in germline cells from two male fetuses affected with fragile X syndrome].
    Duan R; Luo S; Huang W; Li H; Peng Y; Du Q; Wu L
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Oct; 33(5):606-9. PubMed ID: 27577204
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Analysis of CGG variation through 642 meioses in Fragile X families.
    Rifé M; Badenas C; Quintó L; Puigoriol E; Tazón B; Rodriguez-Revenga L; Jiménez L; Sánchez A; Milà M
    Mol Hum Reprod; 2004 Oct; 10(10):773-6. PubMed ID: 15322225
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [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; 44(3):250-6. PubMed ID: 8830601
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Rapid fragile X carrier screening and prenatal diagnosis using a nonradioactive PCR test.
    Brown WT; Houck GE; Jeziorowska A; Levinson FN; Ding X; Dobkin C; Zhong N; Henderson J; Brooks SS; Jenkins EC
    JAMA; 1993 Oct; 270(13):1569-75. PubMed ID: 8371467
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Comparative semi-automated analysis of (CAG) repeats in the Huntington disease gene: use of internal standards.
    Williams LC; Hegde MR; Herrera G; Stapleton PM; Love DR
    Mol Cell Probes; 1999 Aug; 13(4):283-9. PubMed ID: 10441201
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Evaluation of the human fragile X mental retardation 1 polymerase chain reaction reagents to amplify the FMR1 gene: testing in a clinical diagnostic laboratory.
    Nahhas FA; Monroe TJ; Prior TW; Botma PI; Fang J; Snyder PJ; Talbott SL; Feldman GL
    Genet Test Mol Biomarkers; 2012 Mar; 16(3):187-92. PubMed ID: 21992462
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular predictors of cognitive involvement in female carriers of fragile X syndrome.
    Taylor AK; Safanda JF; Fall MZ; Quince C; Lang KA; Hull CE; Carpenter I; Staley LW; Hagerman RJ
    JAMA; 1994 Feb; 271(7):507-14. PubMed ID: 8301764
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Validation of a robust PCR-based assay for quantifying fragile X CGG repeats.
    Kwok YK; Wong KM; Lo FM; Kong GWS; Moore JK; Wu S; Lam STS; Schermer M; Leung TY; Choy KW
    Clin Chim Acta; 2016 May; 456():137-143. PubMed ID: 26947966
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.