Human Genome Epidemiology Literature Finder
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Records 1 - 9 (of 9 Records) |
| Query Trace: Thrombosis and F9[original query] |
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| F9 Malmö, factor IX and deep vein thrombosis. Haematologica 2009 May 94 (5): 693-9. Bezemer Irene D, Arellano Andre R, Tong Carmen H, Rowland Charles M, Ireland Helen A, Bauer Kenneth A, Catanese Joseph, Reitsma Pieter H, Doggen Carine J M, Devlin James J, Rosendaal Frits R, Bare Lance |
| Study of six patients with complete F9 deletion characterized by cytogenetic microarray: role of the SOX3 gene in intellectual disability. Journal of thrombosis and haemostasis : JTH 2016 Oct 14 (10): 1988-1993. Jourdy Y, Chatron N, Carage M-L, Fretigny M, Meunier S, Zawadzki C, Gay V, Negrier C, Sanlaville D, Vinciguerra |
| Genetic profiling revealed an increased risk of venous thrombosis in the Hungarian Roma population. Thrombosis research 2019 5 179 37-44. Fiatal Szilvia, Pikó Péter, Kósa Zsigmond, Sándor János, Ádány Ró |
| Targeted next-generation sequencing reveals novel and known variants of thrombophilia associated genes in Saudi patients with venous thromboembolism. Clinica chimica acta; international journal of clinical chemistry 2021 5 519 247-254. Athar Mohammad, Ghita Ibrahim S, Albagenny Amani A, Abduljaleel Zainularifeen, Shadab Ghulam, Elsendiony Ahmed, Halawani Saeed H, Alkazmi Mohammad M, Alquthami Khalid, Alkhuzae Mohammad M, Althebyani Abdulaziz A, Bogari Neda M, Dannoun Anas, Al-Allaf Faisal |
| Genetic analysis of carrier status in female members of Japanese hemophilia families. Journal of thrombosis and haemostasis : JTH 2021 3 19 (6): 1493-1505. Shinozawa Keiko, Amano Kagehiro, Hagiwara Takeshi, Bingo Masato, Chikasawa Yushi, Inaba Hiroshi, Kinai Ei, Fukutake Katsuyu |
| F9 missense mutations impairing factor IX activation are associated with pleiotropic plasma phenotypes. Journal of thrombosis and haemostasis : JTH 2021 Oct . Branchini Alessio, Morfini Massimo, Lunghi Barbara, Belvini Donata, Radossi Paolo, Bury Loredana, Serino Maria Luisa, Giordano Paola, Cultrera Dorina, Molinari Angelo Claudio, Napolitano Mariasanta, Bigagli Elisabetta, Castaman Giancarlo, Pinotti Mirko, Bernardi Francesco, |
| Results of genetic analysis of 11?341 participants enrolled in the My Life, Our Future hemophilia genotyping initiative in the United States. Journal of thrombosis and haemostasis : JTH 2022 6 20 (9): 2022-2034. Johnsen Jill M, Fletcher Shelley N, Dove Angela, McCracken Haley, Martin Beth K, Kircher Martin, Josephson Neil C, Shendure Jay, Ruuska Sarah E, Valentino Leonard A, Pierce Glenn F, Watson Crystal, Cheng Dunlei, Recht Michael, Konkle Barbara |
| Whole F9 gene sequencing identified deep intronic variations in genetically unresolved hemophilia B patients. Journal of thrombosis and haemostasis : JTH 2023 1 . Dericquebourg Amy, Fretigny Mathilde, Chatron Nicolas, Tardy Brigitte, Zawadzki Christophe, Chambost Hervé, Vinciguerra Christine, Jourdy Yoha |
| The genetic risk factors for cerebral venous thrombosis: a case-control study in a Chinese national comprehensive hospital. Thrombosis journal 2024 6 22 (1): 50. Shaoying Wang, Ming Yao, Xinzhuang Yang, Yicheng Zhu, Bin Pe |
- Page last reviewed:Feb 1, 2024
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