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Author/Creator Boute, O

1. Bilateral periventricular nodular heterotopia in France: frequency of mutations in FLNA, phenotypic heterogeneity and spectrum of mutations. Issue 12 (16th November 2009)

Authors:
Solé, G; Coupry, I; Rooryck, C; Guérineau, E; Martins, F; Devés, S; Hubert, C; Souakri, N; Boute, O; Marchal, C; Faivre, L; Landré, E; Debruxelles, S; Dieux-Coeslier, A; Boulay, C; Chassagnon, S; Michel, V; Routon, M-C; Toutain, A; Philip, N
Journal:
Journal of neurology, neurosurgery and psychiatry
Issue:
Volume 80:Issue 12(2009)
Page Start:
1394
Record Type:
Journal Article
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3. Microdeletion at chromosome 4q21 defines a new emerging syndrome with marked growth restriction, mental retardation and absent or severely delayed speech. Issue 6 (3rd June 2010)

Authors:
Bonnet, C; Andrieux, J; Béri-Dexheimer, M; Leheup, B; Boute, O; Manouvrier, S; Delobel, B; Copin, H; Receveur, A; Mathieu, M; Thiriez, G; Le Caignec, C; David, A; de Blois, M C; Malan, V; Philippe, A; Cormier-Daire, V; Colleaux, L; Flori, E; Dollfus, H
Journal:
Journal of medical genetics
Issue:
Volume 47:Issue 6(2010)
Page Start:
377
Record Type:
Journal Article
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4. PTPN11 mutations in patients with LEOPARD syndrome: a French multicentric experience. Issue 11 (1st November 2004)

Authors:
Keren, B; Hadchouel, A; Saba, S; Sznajer, Y; Bonneau, D; Leheup, B; Boute, O; Gaillard, D; Lacombe, D; Layet, V; Marlin, S; Mortier, G; Toutain, A; Beylot, C; Baumann, C; Verloes, A; Cavé, H
Other Names:
group-author.
Journal:
Journal of medical genetics
Issue:
Volume 41:Issue 11(2004)
Page Start:
e117
Record Type:
Journal Article
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