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Journal Abstract Search

212 related items for PubMed ID: 16999847

  • 61. Congenital structural and functional fibrinogen disorders: a primer for internists.
    Undas A, Casini A.
    Pol Arch Intern Med; 2019 Dec 23; 129(12):913-920. PubMed ID: 31797863
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  • 62. Genetic Analysis of Afibrinogenemia and Hypofibrinogenemia: Novel Mutations in the FGB Gene in the Turkish Population.
    Özkan DT, Sarper N, Akar N.
    Acta Haematol; 2020 Dec 23; 143(6):529-532. PubMed ID: 32289806
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  • 63. Rare deletion from the fibrinogen Bβ gene in a patient with a provoked venous thrombotic event.
    Shen YM, Sarode R, Bhogaraju A, Brennan S.
    Blood Coagul Fibrinolysis; 2011 Oct 23; 22(7):613-5. PubMed ID: 21959590
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  • 64. Dysfibrinogenemia in childhood: two cases of congenital dysfibrinogens.
    Kotlín R, Blažek B, Suttnar J, Malý M, Kvasnička J, Dyr JE.
    Blood Coagul Fibrinolysis; 2010 Oct 23; 21(7):640-8. PubMed ID: 20829681
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  • 66. Clinical features and genetic defect in six index patients with congenital fibrinogen disorders: Three novel mutations with one common mutation in Taiwan's population.
    Shen MC, Wang JD, Tsai W, Lin CY, Lin JS, Kuo SF, Lin PT, Huang YC, Hung MH.
    Haemophilia; 2021 Nov 23; 27(6):1022-1027. PubMed ID: 34460979
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  • 67. Identification and characterization of novel mutations in Chinese patients with congenital fibrinogen disorders.
    Zhou P, Yu M, Peng Y, Ma P, Wan L.
    Blood Cells Mol Dis; 2021 Feb 23; 86():102489. PubMed ID: 32877852
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  • 70. Identification of three FGA mutations in two Chinese families with congenital afibrinogenaemia.
    Fang Y, Dai BT, Wang XF, Fu QH, Dai J, Xie F, Cai XH, Wang HL, Wang ZY.
    Haemophilia; 2006 Nov 23; 12(6):615-20. PubMed ID: 17083511
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  • 71. Congenital afibrinogenemia: mutations leading to premature termination codons in fibrinogen A alpha-chain gene are not associated with the decay of the mutant mRNAs.
    Asselta R, Duga S, Spena S, Santagostino E, Peyvandi F, Piseddu G, Targhetta R, Malcovati M, Mannucci PM, Tenchini ML.
    Blood; 2001 Dec 15; 98(13):3685-92. PubMed ID: 11739173
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  • 72. [Analysis of a family with congenital dysfibrinogenemia caused by an Arg275His mutation in the gamma chain of fibrinogen].
    Yan J, Deng D, Deng X, Luo M, Cheng P, Liao L, Lin F.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Apr 15; 33(2):160-3. PubMed ID: 27060305
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  • 78. A novel frameshift mutation in FGA accounting for congenital afibrinogenemia predicted to encode an aberrant peptide terminating 158 amino acids downstream.
    Robert-Ebadi H, de Moerloose P, El Khorassani M, El Khattab M, Neerman-Arbez M.
    Blood Coagul Fibrinolysis; 2009 Jul 15; 20(5):385-7. PubMed ID: 19417632
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