12 research outputs found
Diagnóstico, tratamento e seguimento do carcinoma medular de tireoide: recomendações do Departamento de Tireoide da Sociedade Brasileira de Endocrinologia e Metabologia
Full text linkTwo DNA alterations of the prothrombin gene at the homozygous state, when present together, cause a severe bleeding disorder
No full text. Molecular characterization of a factor VII deficient patient supports the importance of the second epidermal growth factor-like domain. Haematologica. 89(8):979-84; 2004
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Molecular characterization of a factor Vii deficient patient supports the importance of the second epidermal growth factor-like domain.
No full textMolecular characterization of a factor VII deficient patient supports the importance of the second epidermal growth factor-like domain.
No full textSex modulation of the occurrence of jak2 v617f mutation in patients with splanchnic venous thrombosis. Thromb Res. 2011 Sep;128(3):233-6
No full textSex modulation of the occurrence of jak2 v617f mutation in patients with splanchnic venous thrombosis.
No full textA G-TO-A MUTATION IN IVS-3 OF THE HUMAN GAMMA FIBRINOGEN GENE CAUSING AFIBRINOGENEMIA DUE TO ABNORMAL RNA SPLICING.
No full textA G-to-A mutation in IVS-3 of the human gamma fibrinogen gene causing afibrinogenemia due to abnormal RNA splicing.
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