Factor-V-Leiden Mutation in A Neonate Presenting With Arterial Ischemia

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Recurrent Pregnancy Loss in a Subject with Heterozygote Factor V Leiden Mutation; a Case Report

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Factor V Leiden, MTHFR C677T and Prothrombin Gene Mutation G20210A in Iranian Patients with Venous Thrombosis

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Factor v leiden mutation in reocclusion after intra-arterial thrombolysis.

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recurrent pregnancy loss in a subject with heterozygote factor v leiden mutation; a case report

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ژورنال

عنوان ژورنال: Journal of Pediatrics & Neonatal Care

سال: 2016

ISSN: 2373-4426

DOI: 10.15406/jpnc.2016.05.00186