Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Abnormalities and FGG[original query] |
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[Congenital hypofibrinogenemia associated with a novel mutation in FGG gene]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2015 Jun 32 (3): 331-4. Wang Yingyu, Ding Hongxiang, Hao Xiuping, Zhu Liqing, Yang Lihong, Jin Yanhui, Wang Mingsh |
The Correlation Between Abnormal Uterine Artery Flow in the First Trimester and Genetic Thrombophilic Alteration: A Prospective Case-Controlled Pilot Study. Diagnostics (Basel, Switzerland) 2020 Aug 10 (9): . Vedmedovska Natalija, Bokucava Diana, Kivite-Urtane Anda, Rovite Vita, Zake-Nikitina Liene, Klovins Janis, Fodina Violeta, Donders Gilbert G |
Molecular and clinical profile of congenital fibrinogen disorders in Iran, identification of two novel mutations. International journal of laboratory hematology 2020 7 42 (5): 619-627. Tavasoli Behnaz, Safa Majid, Dorgalaleh Akbar, Ghasemi Jahan B, Rezaei Makhouri Farahnaz, Rezvani Mohammad R, Ahmadi Abbas, Tabibian Shadi, Jazebi Mohammad, Baghaipour Mohammad R, Zaker Farh |
Clinical features and genetic defect in six index patients with congenital fibrinogen disorders: Three novel mutations with one common mutation in Taiwan's population. Haemophilia : the official journal of the World Federation of Hemophilia 2021 8 27 (6): 1022-1027. Shen Ming-Ching, Wang Jiaan-Der, Tsai Woei, Lin Ching-Yeh, Lin Jen-Shiou, Kuo Su-Feng, Lin Po-Te, Huang Ying-Chih, Hung Mei-H |
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