Human Genome Epidemiology Literature Finder
Rare Diseases
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Records 1 - 5 (of 5 Records) |
| Query Trace: Sickle Beta Thalassemia[original query] |
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| Screening for inherited thrombophilia might be warranted among Eastern Mediterranean sickle-beta-0 thalassemia patients. Journal of thrombosis and thrombolysis 2006 Oct 22 (2): 121-3. Isma'eel Hussain, Arnaout M S, Shamseddeen Wael, Mahfouz R, Zeineh N, Jradi Oussama, Taher A |
| Thrombophilic mutations among Southern Iranian patients with sickle cell disease: high prevalence of factor V Leiden. Journal of thrombosis and thrombolysis 2008 Jun 25 (3): 288-92. Rahimi Zohreh, Vaisi-Raygani Asad, Nagel Ronald L, Muniz Adria |
| The relationship between the type of mutation in the globin gene and the type and severity of sickle/beta-thalassemia disease in Jordanian patients. Saudi medical journal 2009 Jul 30 (7): 967-8. El-Akawi Zeyad J, Al-Remawi Hala S, Al-Namarneh Khadijeh |
| Modulating Effect of the -158 ? (C?T) Xmn1 Polymorphism in Indian Sickle Cell Patients. Mediterranean journal of hematology and infectious diseases 2012 4 (1): e2012001. Pandey Sanjay, Pandey Sweta, Mishra Rahasya Mani, Saxena Re |
| Prevalence and Impact of HMOX1 Polymorphism (rs2071746: A?>?T) in Indian Sickle Cell Disease Patients. Journal of laboratory physicians 2023 10 15 (4): 583-589. Hareram Pandey, Kanwaljeet Singh, Ravi Ranjan, Jasmita Dass, Seema Tyagi, Tulika Seth, Renu Saxena, Manoranjan Mahapat |
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