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@Cafadau
Membro desde 1 de agosto de 2013
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Cafadau

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Academic writing ✔ Medical articles ✔ Design ✔ Photography ✔ Anything that requiers skill and vast amounts of general knowledge ✔
$7 USD/hr
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Experiência

Shop assistant

May 2013 - Sep 2013 (4 months)

Educação

Medical student

2011 - 2014 (3 years)

Qualificações

CAE proficiency in english (2011)

British council

Passed the Cambridge CAE exam ( A ) - English level C2

Publicações

Considerations on a familial case of Marfan's syndrome

Marfan syndrome is an autosomal dominant monogenic disease, due to a mutation in fibrillin 1 gene ( FBN1 ), located on chromosome 15q21.1 . Fibrillin 1 mutation causes a hereditary systemic connective tissue disorder that occurs with a frequency of 1 in every 5000 newborns and that affects different tissues and organs with high clinic variability. FBN1 mutation generates a broad phenotypic spectrum, clinical diagnosis relying on the presence of abnormalities in three major systems : the eye ( myopia, sublux

Certificações

  • US English Level 1
    98%

Verificações

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