Effect of mutation type and location on clinical outcome in 1,013 probands with Marfan syndrome or related phenotypes and FBN1 mutations: an international study.
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M Claustres | C Binquet | E. Arbustini | U. Francke | D. Halliday | H. Dietz | C. Béroud | G. Jondeau | K. Holman | M. Claustres | G. Collod-Béroud | A. De Paepe | L. Adès | L. Faivre | C. Boileau | A. Child | K. Mayer | B. Loeys | N. Marziliano | P. Comeglio | B. Callewaert | P. Coucke | K. Mayer | C. Binquet | A. Biggin | A. Paepe | H. Plauchu | C Bonithon-Kopp | H C Dietz | E Arbustini | C Boileau | J. De Backer | G Jondeau | U Francke | E. Gautier | L Faivre | G Collod-Beroud | B L Loeys | A Child | E Gautier | B Callewaert | K Mayer | M Arslan-Kirchner | A Kiotsekoglou | P Comeglio | N Marziliano | D Halliday | C Beroud | C Muti | H Plauchu | P N Robinson | L C Adès | A Biggin | B Benetts | M Brett | K J Holman | J De Backer | P Coucke | A De Paepe | M. Arslan‐Kirchner | A. Kiotsekoglou | M. Brett | J. Backer | C. Muti | P. Robinson | Harry C. Dietz | C. Bonithon‐Kopp | Peter N. Robinson | B. Benetts
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