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Comprehensive mutational analysis of a cohort of Swedish Cornelia de Lange syndrome patients | European Journal of Human Genetics
Madmoiz'elle Mya: son quotidien avec le syndrome cornelia de lange. - Bonsoir !! Mya passe de bonnes vacances ! Entre journée grasse mat', grosse sieste Et levé très tôt mais zéro sieste
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A novel RAD21 mutation in a boy with mild Cornelia de Lange presentation: Further delineation of the phenotype - ScienceDirect
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Cornelia de Lange Syndrome: A Case Report of a Brazilian Boy - Ana C. Scarpelli, Isabela A. Pordeus, Vera L. Resende, Lia S. Castilho, Leandro S. Marques, Saul M. Paiva, 2011
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Medicina | Free Full-Text | De novo NIPBL Mutations in Vietnamese Patients with Cornelia de Lange Syndrome
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