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Journal Abstract Search

620 related items for PubMed ID: 18832909

  • 21. Genetic analysis in Factor XI deficient patients from central China: identification of one novel and seven recurrent mutations.
    Liu H, Wang HF, Tang L, Yang Y, Wang QY, Zeng W, Wu YY, Cheng ZP, Hu B, Guo T, Hu Y.
    Gene; 2015 Apr 25; 561(1):101-6. PubMed ID: 25681615
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  • 22. Molecular characterization of FXI deficiency.
    Berber E.
    Clin Appl Thromb Hemost; 2011 Feb 25; 17(1):27-32. PubMed ID: 20308231
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  • 25. A novel mutation (Gln433Glu) in exon 12 combined with the G insertion in exon 13 causes severe factor XI deficiency in Japanese patients.
    Ishikawa N, Okada S, Sato T, Yasunaga S, Ohtsubo M, Takihara Y, Kobayashi M.
    Blood Coagul Fibrinolysis; 2007 Jul 25; 18(5):519-23. PubMed ID: 17581330
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  • 26. Molecular genetic analysis of the F11 gene in 14 Turkish patients with factor XI deficiency: identification of novel and recurrent mutations and their inheritance within families.
    Colakoglu S, Bayhan T, Tavil B, Keskin EY, Cakir V, Gümrük F, Çetin M, Aytaç S, Berber E.
    Blood Transfus; 2018 Jan 25; 16(1):105-113. PubMed ID: 27723456
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  • 27. A novel heterozygous missense mutation (His127Arg) in a family with inherited cross-reacting material positive factor XI deficiency.
    Castaman G, Giacomelli SH, Tagliaferri A, Rodeghiero F.
    Blood Coagul Fibrinolysis; 2013 Sep 25; 24(6):670-2. PubMed ID: 23571684
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  • 31. High incidence of FXI deficiency in a Spanish town caused by 11 different mutations and the first duplication of F11: Results from the Yecla study.
    Esteban J, de la Morena-Barrio ME, Salloum-Asfar S, Padilla J, Miñano A, Roldán V, Soria JM, Vidal F, Corral J, Vicente V.
    Haemophilia; 2017 Nov 25; 23(6):e488-e496. PubMed ID: 28960694
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  • 32. New observations on factor XI deficiency.
    Salomon O, Seligsohn U.
    Haemophilia; 2004 Oct 25; 10 Suppl 4():184-7. PubMed ID: 15479396
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  • 33. Congenital factor XI deficiency caused by a novel F11 missense variant: a case report.
    Gotovac Jerčić K, Blažeković A, Hančević M, Bilić E, Borovečki F.
    Croat Med J; 2020 Feb 29; 61(1):62-65. PubMed ID: 32118380
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  • 34. A novel F11 mutation in a Korean pediatric patient with recurrent epistaxis.
    Kim J, Kim Y, Shin S, Lyu CJ, Choi JR, Lee KA.
    Blood Coagul Fibrinolysis; 2013 Jun 29; 24(4):433-5. PubMed ID: 23187786
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  • 35. Factor XI deficiency with a novel homozygous mutation Trp599Arg near the C-terminal region.
    Takamiya O, Machida S, Yamamoto M.
    Haematologica; 2005 Jul 29; 90(7):999-1001. PubMed ID: 15996948
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  • 39. First diagnosis of factor XI deficiency in a patient with subarachnoid haemorrhage.
    Vasileiadis I, El-Ali M, Nanas S, Kolias S, Zacharatos P, Christopoulou-Cokkinou V, Kotanidou A.
    Blood Coagul Fibrinolysis; 2009 Jun 29; 20(4):309-13. PubMed ID: 19367158
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  • 40. Identification of a mutation associated with factor XI deficiency in Holstein cattle.
    Marron BM, Robinson JL, Gentry PA, Beever JE.
    Anim Genet; 2004 Dec 29; 35(6):454-6. PubMed ID: 15566468
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