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A highly specific microarray method for point mutation detection.
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A unique mutation underlying carbonic anhydrase II deficiency syndrome in pat...
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A nuclear export signal within the structural Gag protein is required for pro...
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Clinical characteristics of patients with factor V Leiden or prothrombin G202...
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Factor V Leiden prevalence in venous thromboembolism patients.
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Assessment of activated protein C resistance using a new and rapid venom-base...
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Glutamate excitotoxicity is involved in the induction of paralysis in mice af...
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Identification of α-globin chain variants: a report from Iran.
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Computational protein design with a generalized Born solvent model: applicati...
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Risk factors and clinical presentation of venous thromboembolism according to...
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Interrelation of hyperhomocysteinemia and inherited risk factors for venous t...
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High frequency of factor V Leiden in surgical patients with symptomatic venou...
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Fibrinogen Aalpha-Thr312Ala and factor XIII-A Val34Leu polymorphisms in idiop...
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Characterization of a hepatitis B and hepatitis delta virus receptor binding ...
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Eight previously unidentified mutations found in the OA1 ocular albinism gene.
BACKGROUND: Ocular albinism type 1 (OA1) is an X-linked ocular disorder characterized by a severe reduction in visual acuity, nystagmus, hypopigmentation of the... -
Hematologically important mutations: the autosomal recessive forms of chronic...
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First report on the co-inheritance of beta-globin IVS-I-5 (G-->C) thalassemia...
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Prevalence of molecular markers of Plasmodium falciparum drug resistance in D...
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A novel function for spumaretrovirus integrase: an early requirement for inte...
Retroviral integration is central to viral persistence and pathogenesis, cancer as well as host genome evolution. However, it is unclear why integration appears... -
Comparative proteomics as a new tool for exploring human mitochondrial tRNA d...
International audience
