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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English | 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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Mireille Claustres
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Gwenaëlle Collod-Béroud
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Claire Bonithon-Kopp
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Alice Masurel-Paulet
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Laurence Faivre
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Anne H Child
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Chantal Stheneur
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Christine Binquet
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Elodie Gautier
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Bertrand Chevallier
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Frédéric Huet
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Karin Mayer
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Mine Arslan-Kirchner
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Anatoli Kiotsekoglou
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Paolo Comeglio
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Maurizia Grasso
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Dorothy J Halliday
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Lesley Adès
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Paul Coucke
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Uta Francke
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Anne De Paepe
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Guillaume Jondeau
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1 January 2009
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123
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391-398
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