BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

161 related articles for article (PubMed ID: 26741412)

  • 1. Identification of microsatellite markers <1 Mb from the FMR1 CGG repeat and development of a single-tube tetradecaplex PCR panel of highly polymorphic markers for preimplantation genetic diagnosis of fragile X syndrome.
    Chen M; Zhao M; Lee CG; Chong SS
    Genet Med; 2016 Sep; 18(9):869-75. PubMed ID: 26741412
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Single-tube tetradecaplex panel of highly polymorphic microsatellite markers < 1 Mb from F8 for simplified preimplantation genetic diagnosis of hemophilia A.
    Zhao M; Chen M; Tan ASC; Cheah FSH; Mathew J; Wong PC; Chong SS
    J Thromb Haemost; 2017 Jul; 15(7):1473-1483. PubMed ID: 28345288
    [TBL] [Abstract][Full Text] [Related]  

  • 3. FMR1 CGG repeat expansion mutation detection and linked haplotype analysis for reliable and accurate preimplantation genetic diagnosis of fragile X syndrome.
    Rajan-Babu IS; Lian M; Cheah FSH; Chen M; Tan ASC; Prasath EB; Loh SF; Chong SS
    Expert Rev Mol Med; 2017 Jul; 19():e10. PubMed ID: 28720156
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Improving preimplantation genetic diagnosis for Fragile X syndrome: two new powerful single-round multiplex indirect and direct tests.
    Kieffer E; Nicod JC; Gardes N; Kastner C; Becker N; Celebi C; Pirrello O; Rongières C; Koscinski I; Gosset P; Moutou C
    Eur J Hum Genet; 2016 Feb; 24(2):221-7. PubMed ID: 25966634
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Identification of Novel Microsatellite Markers <1 Mb from the HTT CAG Repeat and Development of a Single-Tube Tridecaplex PCR Panel of Highly Polymorphic Markers for Preimplantation Genetic Diagnosis of Huntington Disease.
    Zhao M; Chen M; Lee CG; Chong SS
    Clin Chem; 2016 Aug; 62(8):1096-105. PubMed ID: 27335079
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Preimplantation genetic diagnosis for fragile X syndrome: is there increased transmission of abnormal FMR1 alleles among female heterozygotes?
    Reches A; Malcov M; Ben-Yosef D; Azem F; Amit A; Yaron Y
    Prenat Diagn; 2009 Jan; 29(1):57-61. PubMed ID: 19097038
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Identification of novel microsatellite markers <1 Mb from the HBB gene and development of a single-tube pentadecaplex PCR panel of highly polymorphic markers for preimplantation genetic diagnosis of beta-thalassemia.
    Chen M; Tan AS; Cheah FS; Saw EE; Chong SS
    Electrophoresis; 2015 Dec; 36(23):2914-24. PubMed ID: 26331357
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Multiple displacement amplification for preimplantation genetic diagnosis of fragile X syndrome.
    Lee HS; Kim MJ; Lim CK; Cho JW; Song IO; Kang IS
    Genet Mol Res; 2011 Nov; 10(4):2851-9. PubMed ID: 22095609
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Single-Tube Dodecaplex PCR Panel of Polymorphic Microsatellite Markers Closely Linked to the
    Lian M; Zhao M; Lee CG; Chong SS
    Clin Chem; 2017 Jun; 63(6):1127-1140. PubMed ID: 28428361
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Preimplantation genetic diagnosis of the fragile X syndrome by use of linked polymorphic markers.
    Apessos A; Abou-Sleiman PM; Harper JC; Delhanty JD
    Prenat Diagn; 2001 Jun; 21(6):504-11. PubMed ID: 11438958
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A Robust Polymerase Chain Reaction-based Assay for Quantifying Cytosine-guanine-guanine Trinucleotide Repeats in Fragile X Mental Retardation-1 Gene.
    Wang H; Zhu X; Gui B; Cheung WC; Shi M; Yang Z; Kwok KY; Lim R; Pietilä S; Zhu Y; Choy KW
    J Vis Exp; 2019 Sep; (151):. PubMed ID: 31566610
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Preimplantation genetic diagnosis for fragile X syndrome using multiplex nested PCR.
    Malcov M; Naiman T; Yosef DB; Carmon A; Mey-Raz N; Amit A; Vagman I; Yaron Y
    Reprod Biomed Online; 2007 Apr; 14(4):515-21. PubMed ID: 17425837
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Chromosome fragility at FRAXA in human cleavage stage embryos at risk for fragile X syndrome.
    Verdyck P; Berckmoes V; De Vos A; Verpoest W; Liebaers I; Bonduelle M; De Rycke M
    Am J Med Genet A; 2015 Oct; 167A(10):2306-13. PubMed ID: 25953684
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Simultaneous Screening of the FRAXA and FRAXE Loci for Rapid Detection of FMR1 CGG and/or AFF2 CCG Repeat Expansions by Triplet-Primed PCR.
    Liu T; Wang FS; Cheah FSH; Gu Y; Shaw M; Law HY; Tay SKH; Lee CG; Nelson DL; Gecz J; Chong SS
    J Mol Diagn; 2021 Aug; 23(8):941-951. PubMed ID: 34111553
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Establishment of FXS-A9 panel with a single human X chromosome from fragile X syndrome-associated individual.
    Nakayama Y; Adachi K; Shioda N; Maeta S; Nanba E; Kugoh H
    Exp Cell Res; 2021 Jan; 398(2):112419. PubMed ID: 33296661
    [TBL] [Abstract][Full Text] [Related]  

  • 16. CGG-repeat dynamics and
    Zhou Y; Kumari D; Sciascia N; Usdin K
    Mol Autism; 2016; 7():42. PubMed ID: 27713816
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Clinical Genetic Testing for Fragile X Syndrome by Polymerase Chain Reaction Amplification and Southern Blot Analyses.
    Cai X; Arif M; Wan H; Kornreich R; Edelmann LJ
    Methods Mol Biol; 2019; 1942():11-27. PubMed ID: 30900172
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Qualitative assessment of FMR1 (CGG)n triplet repeat status in normal, intermediate, premutation, full mutation, and mosaic carriers in both sexes: implications for fragile X syndrome carrier and newborn screening.
    Hantash FM; Goos DG; Tsao D; Quan F; Buller-Burckle A; Peng M; Jarvis M; Sun W; Strom CM
    Genet Med; 2010 Mar; 12(3):162-73. PubMed ID: 20168238
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Contraction of fully expanded FMR1 alleles to the normal range: predisposing haplotype or rare events?
    Maia N; Loureiro JR; Oliveira B; Marques I; Santos R; Jorge P; Martins S
    J Hum Genet; 2017 Feb; 62(2):269-275. PubMed ID: 27784894
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Re-examination of factors associated with expansion of CGG repeats using a single nucleotide polymorphism in FMR1.
    Gunter C; Paradee W; Crawford DC; Meadows KA; Newman J; Kunst CB; Nelson DL; Schwartz C; Murray A; Macpherson JN; Sherman SL; Warren ST
    Hum Mol Genet; 1998 Nov; 7(12):1935-46. PubMed ID: 9811938
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.