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PUBMED FOR HANDHELDS

Journal Abstract Search


117 related items for PubMed ID: 27335079

  • 1. 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
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  • 3. 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
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  • 4. 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
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  • 5. 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
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  • 7. First preimplantation genetic testing case for monogenic disease in Latvia.
    Perminov D, Voložonoka L, Korņejeva L, Jokste-Pțmane E, Blumberga A, Krasucka S, Seimuškina N, Kovaļova I, Fodina V.
    Gynecol Endocrinol; 2017 Sep; 33(sup1):47-49. PubMed ID: 29264979
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  • 11. One-step multiplex polymerase chain reaction for preimplantation genetic diagnosis of Huntington disease.
    Peciña A, Lozano Arana MD, García-Lozano JC, Borrego S, Antiñolo G.
    Fertil Steril; 2010 May 01; 93(7):2411-2. PubMed ID: 19423106
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  • 12. Identification of Novel Microsatellite Markers Flanking the SMN1 and SMN2 Duplicated Region and Inclusion Into a Single-Tube Tridecaplex Panel for Haplotype-Based Preimplantation Genetic Testing of Spinal Muscular Atrophy.
    Zhao M, Lian M, Cheah FSH, Tan ASC, Agarwal A, Chong SS.
    Front Genet; 2019 May 01; 10():1105. PubMed ID: 31781167
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  • 14. Expanding the Spectrum of Genes Involved in Huntington Disease Using a Combined Clinical and Genetic Approach.
    Mariani LL, Tesson C, Charles P, Cazeneuve C, Hahn V, Youssov K, Freeman L, Grabli D, Roze E, Noël S, Peuvion JN, Bachoud-Levi AC, Brice A, Stevanin G, Durr A.
    JAMA Neurol; 2016 Sep 01; 73(9):1105-14. PubMed ID: 27400454
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