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Results of search for 'au:"de Backer, J"', page 7 of 7
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Authors
André, C
Arbustini, E
Arslan-Kirchner, M
Beroud, C
Binquet, C
Boileau, C
Bonithon-Kopp, C
Child, A
Convents, A
Coucke, P
DE BACKER, J
De Backer, J
De Backer, J P
De Backer, W
De Keyser, J
De Paepe, A
De Vos, H
Ebinger, G
Vanderheyden, P M
Vauquelin, G
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121.
The new Ghent criteria for Marfan syndrome: what do they change?
[electronic resource]
by
Faivre, L
Collod-Beroud, G
Adès, L
Arbustini, E
Child, A
Callewaert, B L
Loeys, B
Binquet, C
Gautier, E
Mayer, K
Arslan-Kirchner, M
Grasso, M
Beroud, C
Hamroun, D
Bonithon-Kopp, C
Plauchu, H
Robinson, P N
De Backer, J
Coucke, P
Francke, U
Bouchot, O
Wolf, J E
Stheneur, C
Hanna, N
Detaint, D
De Paepe, A
Boileau, C
Jondeau, G
Producer:
20120807
In:
Clinical genetics
vol. 81
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122.
Clinical and mutation-type analysis from an international series of 198 probands with a pathogenic FBN1 exons 24-32 mutation.
[electronic resource]
by
Faivre, L
Collod-Beroud, G
Callewaert, B
Child, A
Binquet, C
Gautier, E
Loeys, B L
Arbustini, E
Mayer, K
Arslan-Kirchner, M
Stheneur, C
Kiotsekoglou, A
Comeglio, P
Marziliano, N
Wolf, J E
Bouchot, O
Khau-Van-Kien, P
Beroud, C
Claustres, M
Bonithon-Kopp, C
Robinson, P N
Adès, L
De Backer, J
Coucke, P
Francke, U
De Paepe, A
Jondeau, G
Boileau, C
Producer:
20090508
In:
European journal of human genetics : EJHG
vol. 17
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123.
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.
[electronic resource]
by
Faivre, L
Collod-Beroud, G
Loeys, B L
Child, A
Binquet, C
Gautier, E
Callewaert, B
Arbustini, E
Mayer, K
Arslan-Kirchner, M
Kiotsekoglou, A
Comeglio, P
Marziliano, N
Dietz, H C
Halliday, D
Beroud, C
Bonithon-Kopp, C
Claustres, M
Muti, C
Plauchu, H
Robinson, P N
Adès, L C
Biggin, A
Benetts, B
Brett, M
Holman, K J
De Backer, J
Coucke, P
Francke, U
De Paepe, A
Jondeau, G
Boileau, C
Producer:
20071004
In:
American journal of human genetics
vol. 81
Online resources:
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