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Journal Abstract Search

178 related items for PubMed ID: 28345288

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. Preimplantation genetic diagnosis for hemophilia A using indirect linkage analysis and direct genotyping approaches.
    Laurie AD, Hill AM, Harraway JR, Fellowes AP, Phillipson GT, Benny PS, Smith MP, George PM.
    J Thromb Haemost; 2010 Apr; 8(4):783-9. PubMed ID: 20102489
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  • 4. 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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  • 6. 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
    [Abstract] [Full Text] [Related]

  • 7. Inverse PCR to perform long-distance haplotyping: main applications to improve preimplantation genetic diagnosis in hemophilia.
    Abelleyro MM, Marchione VD, Palmitelli M, Radic CP, Neme D, Larripa IB, Medina-Acosta E, De Brasi CD, Rossetti LC.
    Eur J Hum Genet; 2019 Apr; 27(4):603-611. PubMed ID: 30626931
    [Abstract] [Full Text] [Related]

  • 8. 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
    [Abstract] [Full Text] [Related]

  • 9. High-resolution combined linkage physical map of short tandem repeat loci on human chromosome band Xq28 for indirect haemophilia A carrier detection.
    Machado FB, Medina-Acosta E.
    Haemophilia; 2009 Jan; 15(1):297-308. PubMed ID: 18752533
    [Abstract] [Full Text] [Related]

  • 10. Preimplantation genetic testing (PGT) for hemophilia A: Experience from one center.
    Bui TMP, Tran VK, Nguyen TTH, Le TP, Nguyen TM, Tran HA, Luu VD, Nguyen MH, Bui TH, Van Ta T, Tran TH.
    Taiwan J Obstet Gynecol; 2022 Nov; 61(6):1009-1014. PubMed ID: 36427965
    [Abstract] [Full Text] [Related]

  • 11. [New efficient extragenic microsatellite markers for hemophilia A carrier state diagnostics].
    Surin VL, Luk'ianenko AV, Luchinina IuA.
    Genetika; 2007 Jun; 43(6):831-40. PubMed ID: 17853810
    [Abstract] [Full Text] [Related]

  • 12. Four Decades of Carrier Detection and Prenatal Diagnosis in Hemophilia A: Historical Overview, State of the Art and Future Directions.
    Dardik R, Janczar S, Lalezari S, Avishai E, Levy-Mendelovich S, Barg AA, Martinowitz U, Babol-Pokora K, Mlynarski W, Kenet G.
    Int J Mol Sci; 2023 Jul 24; 24(14):. PubMed ID: 37511607
    [Abstract] [Full Text] [Related]

  • 13. Polar body diagnosis for hemophilia a using multiplex PCR for linked polymorphic markers.
    Tomi D, Griesinger G, Schultze-Mosgau A, Eckhold J, Schöpper B, Al-Hasani S, Diedrich K, Schwinger E.
    J Histochem Cytochem; 2005 Mar 24; 53(3):277-80. PubMed ID: 15750001
    [Abstract] [Full Text] [Related]

  • 14. Single-Tube Dodecaplex PCR Panel of Polymorphic Microsatellite Markers Closely Linked to the DMPK CTG Repeat for Preimplantation Genetic Diagnosis of Myotonic Dystrophy Type 1.
    Lian M, Zhao M, Lee CG, Chong SS.
    Clin Chem; 2017 Jun 24; 63(6):1127-1140. PubMed ID: 28428361
    [Abstract] [Full Text] [Related]

  • 15. A highly informative, multiplexed assay for the indirect detection of hemophilia A using five-linked microsatellites.
    Harraway JR, Smith MP, George PM.
    J Thromb Haemost; 2006 Mar 24; 4(3):587-90. PubMed ID: 16460441
    [Abstract] [Full Text] [Related]

  • 16. Improved criterion-referenced assessment in indirect tracking of haemophilia A using a 0.23 cM-resolution dense polymorphic marker set.
    Machado FB, Duarte LP, Medina-Acosta E.
    Haemophilia; 2009 Sep 24; 15(5):1135-42. PubMed ID: 19624762
    [Abstract] [Full Text] [Related]

  • 17. 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; 19():e10. PubMed ID: 28720156
    [Abstract] [Full Text] [Related]

  • 18. Single cell co-amplification of polymorphic markers for the indirect preimplantation genetic diagnosis of hemophilia A, X-linked adrenoleukodystrophy, X-linked hydrocephalus and incontinentia pigmenti loci on Xq28.
    Gigarel N, Frydman N, Burlet P, Kerbrat V, Steffann J, Frydman R, Munnich A, Ray PF.
    Hum Genet; 2004 Feb 19; 114(3):298-305. PubMed ID: 14673643
    [Abstract] [Full Text] [Related]

  • 19. Single-tube nonaplex microsatellite PCR panel for preimplantation genetic diagnosis of Hb Bart's hydrops fetalis syndrome.
    Chen M, Chan JK, Nadarajah S, Tan AS, Chan ML, Mathew J, Saw EE, Lim C, Wong W, Cheah FS, Law HY, Wong PC, Chong SS.
    Prenat Diagn; 2015 Jun 19; 35(6):534-43. PubMed ID: 25641621
    [Abstract] [Full Text] [Related]

  • 20. Genotyping of intron 22 inversion of factor VIII gene for diagnosis of hemophilia A by inverse-shifting polymerase chain reaction and capillary electrophoresis.
    Pan TY, Wang CC, Shih CJ, Wu HF, Chiou SS, Wu SM.
    Anal Bioanal Chem; 2014 Sep 19; 406(22):5447-54. PubMed ID: 24994666
    [Abstract] [Full Text] [Related]

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