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The Koolen-de Vries syndrome: a phenotypic comparison of patients with a 17q21.31 microdeletion versus a KANSL1 sequence variant
2015
185 citations
Journal Article
bronze Open Access
Field-Weighted Citation Impact:
15.81
The Koolen-de Vries syndrome: a phenotypic comparison of patients with a 17q21.31 microdeletion versus a KANSL1 sequence variant | Researchclopedia
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