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Clinical and molecular characterization of 17q21.31 microdeletion syndrome in 14 French patients with mental retardation.European Journal of Medical Genetics, 2011, 54 (2), pp.144-51. ⟨10.1016/j.ejmg.2010.11.003⟩
Journal articles
inserm-00541962v1
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Identification of gene copy number variations in patients with mental retardation using array-CGH: Novel syndromes in a large French series.European Journal of Medical Genetics, 2010, 53 (2), pp.66-75. ⟨10.1016/j.ejmg.2009.10.002⟩
Journal articles
istex
inserm-00434932v1
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