Pages that link to "Q46876638"
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The following pages link to Clinical manifestations of the prothrombin G20210A mutation in children: a pediatric coagulation consortium study (Q46876638):
Displaying 8 items.
- Current proceedings of childhood stroke (Q34572329) (← links)
- Thrombophilia testing in a tertiary paediatric hospital: Indications, outcomes and appropriateness. (Q38481403) (← links)
- Venous Thromboembolic Disease in Children and Adolescents (Q38954315) (← links)
- Stroke in the fetus and neonate (Q40292913) (← links)
- Genetic Risk Factors in Venous Thromboembolism. (Q40577579) (← links)
- The influence of risk factors in promoting thrombosis during childhood: the role of acquired factors (Q43689806) (← links)
- Bilateral Superficial Femoral Artery Thrombosis in a 15-Year-Old Caucasian Male with Homozygous Prothrombin G20210A Genotype and Associated Antiphospholipid Syndrome (Q46699558) (← links)
- Cerebral venous sinus thrombosis in a neonate with homozygous prothrombin G20210A genotype (Q81042683) (← links)