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Publication Detail
A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders
  • Publication Type:
    Journal article
  • Publication Sub Type:
    Article
  • Authors:
    Simeoni I, Stephens JC, Hu F, Deevi SVV, Megy K, Bariana TK, Lentaigne C, Schulman S, Sivapalaratnam S, Vries MJA, Westbury SK, Greene D, Papadia S, Alessi M-C, Attwood AP, Ballmaier M, Baynam G, Bermejo E, Bertoli M, Bray PF, Bury L, Cattaneo M, Collins P, Daugherty LC, Favier R, French DL, Furie B, Gattens M, Germeshausen M, Ghevaert C, Goodeve AC, Guerrero JA, Hampshire DJ, Hart DP, Heemskerk JWM, Henskens YMC, Hill M, Hogg N, Jolley JD, Kahr WH, Kelly AM, Kerr R, Kostadima M, Kunishima S, Lambert MP, Liesner R, Lopez JA, Mapeta RP, Mathias M, Millar CM, Nathwani A, Neerman-Arbez M, Nurden AT, Nurden P, Othman M, Peerlinck K, Perry DJ, Poudel P, Reitsma P, Rondina MT, Smethurst PA, Stevenson W, Szkotak A, Tuna S, van Geet C, Whitehorn D, Wilcox DA, Zhang B, Revel-Vilk S, Gresele P, Bellissimo DB, Penkett CJ, Laffan MA, Mumford AD, Rendon A, Gomez K, Freson K, Ouwehand WH, Turro E
  • Publisher:
    AMER SOC HEMATOLOGY
  • Publication date:
    09/06/2016
  • Pagination:
    2791, 2803
  • Journal:
    BLOOD
  • Volume:
    127
  • Issue:
    23
  • Status:
    Published
  • Print ISSN:
    0006-4971
  • Language:
    English
  • Keywords:
    Science & Technology, Life Sciences & Biomedicine, Hematology, VON-WILLEBRAND-DISEASE, WISKOTT-ALDRICH SYNDROME, FACTOR-VIII GENE, UNITED-KINGDOM, GENOME, MANAGEMENT, MUTATIONS, LINKAGE, POLYMORPHISMS, POPULATION
Abstract
No abstract found
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