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+1040 C/T polymorphism in coding region of thrombin-activatable fibrinolysis inhibitor gene and the risk of idiopathic recurrent fetal loss
| Naziv: | +1040 C/T polymorphism in coding region of thrombin-activatable fibrinolysis inhibitor gene and the risk of idiopathic recurrent fetal loss | Autori: | Pruner, Iva |
Godina: | 2010 | Publikacija: | Blood Coagulation & Fibrinolysis | ISSN: | 0957-5235 Blood Coagulation and Fibrinolysis Pretraži identifikator |
Izdavač: | Lippincott Williams & Wilkins, Philadelphia | Tip rezultata: | Naučni članak | Kolacija: | vol. 21 br. 7 str. 679-682 | DOI: | 10.1097/mbc.0b013e32833e426d | WoS-ID: | 000282483500011 | Scopus-ID: | 2-s2.0-77958155397 | PMID: | 20729722 | URI: | https://enauka.gov.rs/handle/123456789/204699 https://imagine.imgge.bg.ac.rs/handle/123456789/441 |
Projekat: | Структурални елементи генома у модулацији фенотипа | Izvor metapodataka: | Migracija | M-kategorija: | 22M22 - Međunarodni časopis kategorije M22 |
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