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Journal Abstract Search

160 related items for PubMed ID: 29264979

  • 1. 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; 33(sup1):47-49. PubMed ID: 29264979
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  • 4. Live births following preimplantation genetic testing for dynamic mutation diseases by karyomapping: a report of three cases.
    Shi D, Xu J, Niu W, Liu Y, Shi H, Yao G, Shi S, Li G, Song W, Jin H, Sun Y.
    J Assist Reprod Genet; 2020 Mar; 37(3):539-548. PubMed ID: 32124191
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  • 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
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  • 6. Huntington's Disease: Relationship Between Phenotype and Genotype.
    Sun YM, Zhang YB, Wu ZY.
    Mol Neurobiol; 2017 Jan; 54(1):342-348. PubMed ID: 26742514
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  • 7. 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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  • 13. Preimplantation genetic diagnosis for Huntington's disease with exclusion testing.
    Sermon K, De Rijcke M, Lissens W, De Vos A, Platteau P, Bonduelle M, Devroey P, Van Steirteghem A, Liebaers I.
    Eur J Hum Genet; 2002 Oct 01; 10(10):591-8. PubMed ID: 12357329
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  • 17. A Novel Triplet-Primed PCR Assay to Detect the Full Range of Trinucleotide CAG Repeats in the Huntingtin Gene (HTT).
    De Luca A, Morella A, Consoli F, Fanelli S, Thibert JR, Statt S, Latham GJ, Squitieri F.
    Int J Mol Sci; 2021 Feb 08; 22(4):. PubMed ID: 33567536
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  • 18. Preimplantation diagnosis for Huntington's disease (HD): clinical application and analysis of the HD expansion in affected embryos.
    Sermon K, Goossens V, Seneca S, Lissens W, De Vos A, Vandervorst M, Van Steirteghem A, Liebaers I.
    Prenat Diagn; 1998 Dec 08; 18(13):1427-36. PubMed ID: 9949443
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  • 19. HTT gene intermediate alleles in neurodegeneration: evidence for association with Alzheimer's disease.
    Menéndez-González M, Clarimón J, Rosas-Allende I, Blázquez M, San Martín ES, García-Fernández C, Lleó A, Dols-Icardo O, Illán-Gala I, Morís G, Ribacoba R, Álvarez V, Martínez C.
    Neurobiol Aging; 2019 Apr 08; 76():215.e9-215.e14. PubMed ID: 30583877
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  • 20. Chromosomal instability during neurogenesis in Huntington's disease.
    Ruzo A, Croft GF, Metzger JJ, Galgoczi S, Gerber LJ, Pellegrini C, Wang H, Fenner M, Tse S, Marks A, Nchako C, Brivanlou AH.
    Development; 2018 Jan 29; 145(2):. PubMed ID: 29378824
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