Clinical and molecular study of 320 children with Marfan syndrome and related type I fibrillinopathies in a series of 1009 probands with pathogenic FBN1 mutations (Q43625160)

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Clinical and molecular study of 320 children with Marfan syndrome and related type I fibrillinopathies in a series of 1009 probands with pathogenic FBN1 mutations
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    Clinical and molecular study of 320 children with Marfan syndrome and related type I fibrillinopathies in a series of 1009 probands with pathogenic FBN1 mutations (English)
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    Chantal Stheneur
    Christine Binquet
    Bertrand Chevallier
    Frédéric Huet
    Mine Arslan-Kirchner
    Anatoli Kiotsekoglou
    Maurizia Grasso
    Dorothy J Halliday
    Guillaume Jondeau

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