Publications by authors named "O Raoul"

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Electro-clinical features in epileptic children with chromosome 15q duplication syndrome.
M-T Dangles, V Malan, G Dumas, S Romana, O Raoul

Clin Neurophysiol· May 2021

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New insights into genotype-phenotype correlation for GLI3 mutations.
Florence Démurger, Amale Ichkou, Soumaya Mougou-Zerelli, Martine Le Merrer, Géraldine Goudefroye, Odile Raoul

Eur J Hum Genet· January 2015

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Phenotype-genotype correlations in 17 new patients with an Xp11.23p11.22 microduplication and review of the literature.
Mathilde Nizon, Joris Andrieux, Caroline Rooryck, Marie-Christine de Blois, Emilie Bourel-Ponchel, Odile Raoul

Am J Med Genet A· January 2015

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19q13.11 deletion syndrome: a novel clinically recognisable genetic condition identified by array comparative genomic hybridisation.
V Malan, O Raoul, H V Firth, G Royer, C Turleau

J Med Genet· September 2009

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Sporadic case of unusual facies, cerebral vascular anomalies and developmental delay.
Marta Bertoli, Nathalie Boddaert, Odile Raoul, Jeanne Amiel, Stanislas Lyonnet

Clin Dysmorphol· April 2009

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