These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

133 related items for PubMed ID: 37906135

  • 1. [Genetic analysis of a Chinese pedigree affected with Congenital dysfibrinogenemia due to variant of FGG gene].
    Shao X, Ma J, Wang Z, Sun M, Huang Z, Jiang Z, Liu X, Li S, Liu Y.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Nov 10; 40(11):1324-1329. PubMed ID: 37906135
    [Abstract] [Full Text] [Related]

  • 2. [Mutation analysis of a FGG gene causing hereditary abnormal fibrinogen].
    Jiang L, Zhang Q, Xu W, Zhang Y.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Dec 10; 35(6):812-814. PubMed ID: 30512152
    [Abstract] [Full Text] [Related]

  • 3. [Analysis of a pedigree affected with congenital dysfibrinogenemia due to a novel Gly31Glu mutation of FGA gene].
    Wang X, Yang X, Yang W, Shu K, Li F, Liu J, Zhang Z, Li S, Jiang M.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Sep 10; 36(9):901-904. PubMed ID: 31515786
    [Abstract] [Full Text] [Related]

  • 4. [A Family with Congenital Dysfibrinogenemia and Blood Transfusion].
    Liao XC, Zhang SS, Yang ZJ, Zhu CL, Huang HN, Luo RX, Li SN, Xie HQ, Li HL, Mo ZN.
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2023 Oct 10; 31(5):1469-1474. PubMed ID: 37846702
    [Abstract] [Full Text] [Related]

  • 5. [Genetic analysis of two Chinese pedigrees affected with Hereditary hypofibrinemia due to missense variants].
    Zheng X, Chen Y, Wen M, Jin Y, Zeng M, Jia K, Chen Y, Wang M, Yang L.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Mar 10; 40(3):276-281. PubMed ID: 36854400
    [Abstract] [Full Text] [Related]

  • 6. [Congenital hypofibrinogenemia associated with a novel mutation in FGG gene].
    Wang Y, Ding H, Hao X, Zhu L, Yang L, Jin Y, Wang M.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Jun 10; 32(3):331-4. PubMed ID: 26037343
    [Abstract] [Full Text] [Related]

  • 7. [A case of inherited afibrinogenemia caused by an IVS7-12A>G splice mutation of FGG gene].
    Wang X, Yang X, Wang J, Shu K, Li F, Yang W, Ruan J, Wang S, Jiang M.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Dec 10; 37(12):1391-1394. PubMed ID: 33306830
    [Abstract] [Full Text] [Related]

  • 8. [Clinical and genetic analysis of 8 Chinese pedigrees with inherited dysfibrinogenemia].
    Jiang M, Wang X, Shu K, Jiang W, Huang Y, Lin Y, Li S, Hu Y.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Apr 10; 31(2):134-9. PubMed ID: 24711018
    [Abstract] [Full Text] [Related]

  • 9. [Analysis of a pedigree affected with congenital hypofibrinogenemia due to heterozygous Ser313Ile mutation of fibrinogen γ chain gene].
    Zhu L, Zhao M, Cheng X, Yu D, Li X, Xu F, Wang J, Wang M.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Apr 10; 35(2):179-183. PubMed ID: 29652987
    [Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11. [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 10; 33(2):160-3. PubMed ID: 27060305
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. [Fibrinogen gamma-chain mutation, p.Ile171His, leads to hereditary hypofibrinogenemia].
    Liu JX, Wang CJ, Dai JH, Zhang MX, Lyu B, Jiang B.
    Zhonghua Nei Ke Za Zhi; 2022 Feb 01; 61(2):172-176. PubMed ID: 35090252
    [Abstract] [Full Text] [Related]

  • 14. [Analysis of two pedigrees affected with inherited dysfibrinogenemia due to a novel c.1115 T>A variant of the FGB gene].
    Wang X, Yao Y, Lin S, Wang J, Shu K, Ai X, Jiang M.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2022 Jun 10; 39(6):587-591. PubMed ID: 35773760
    [Abstract] [Full Text] [Related]

  • 15. [Phenotype and genotype analyses of two pedigrees with inherited fibrinogen deficiency].
    Jia KQ, Su ZX, Chen HL, Zheng XY, Zeng ML, Zhang K, Ye LY, Yang LL, Jin YH, Wang MS.
    Zhonghua Xue Ye Xue Za Zhi; 2023 Nov 14; 44(11):930-935. PubMed ID: 38185523
    [Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. 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 14; 12(6):615-20. PubMed ID: 17083511
    [Abstract] [Full Text] [Related]

  • 18. [Congenital afibrinogenemia caused by a novel insertion mutation in the FGB gene].
    Zhang J, Zhao XJ, Wang ZY, Yu ZQ, Cao LJ, Ma ZN, Zhang J, Zhang W, Bai X, Ruan CG.
    Zhonghua Xue Ye Xue Za Zhi; 2013 Sep 14; 34(9):751-6. PubMed ID: 24103871
    [Abstract] [Full Text] [Related]

  • 19. [Genetic analysis of a Chinese pedigree affected with Congenital coagulation factor XII deficiency due to a c.1A>G start codon variant of F12 gene].
    Ji W, Lin S, Chen J, Jin C, Lin X, Ye Z, Qiu L, Qian D.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 May 10; 40(5):547-551. PubMed ID: 37102287
    [Abstract] [Full Text] [Related]

  • 20. [Genetic analysis of an inherited afibrinogenemia family caused by a novel frameshift mutation in FGA].
    Xue F, Ge J, Gu DS, DU WT, Sui T, Zhao HF, Zhang L, Yang RC.
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2009 Aug 10; 17(4):1021-5. PubMed ID: 19698251
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 7.