PROTHROMBIN G20210A MUTATION IN TURKISH CHILDREN WITH THROMBOSIS AND THE FREQUENCY OF PROTHROMBIN C20209T
Author:
Publisher
Informa UK Limited
Subject
Oncology,Hematology,Pediatrics, Perinatology and Child Health
Link
http://www.tandfonline.com/doi/pdf/10.1080/08880010590935202
Reference7 articles.
1. Clinical manifestations of the prothrombin G20210A mutation in children: a pediatric coagulation consortium study
2. Prothrombin G20210A Gene Mutation and Further Prothrombotic Risk Factors in Childhood Thrombophilia
3. The 20210 G → A mutation in the 3′-untranslated region of the prothrombin gene and the risk for arterial thrombotic disease
4. Factor V1691 G-A, Prothrombin 20210 G-A, and Methylenetetrahydrofolate Reductase 677 C-T Variants in Turkish Children With Cerebral Infarct
5. Geographic Distribution of the 20210 G to A Prothrombin Variant
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3. Prothrombin G20210A Mutation, Hypogonadotropic Hypogonadism, and Generalized Vitiligo-Related Ischemic Stroke in a Young Adult;International Journal of Neuroscience;2010-05
4. INCIDENCE OF AND RISK FACTORS FOR CHILDHOOD THROMBOSIS: A Single-Center Experience in Ankara, Turkey;Pediatric Hematology and Oncology;2009-01
5. Hereditary Thrombophilic Factors in Stroke Due to Cerebral Infarct;The American Journal of the Medical Sciences;2009-01
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