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Intragenic KANSL1 mutations and chromosome 17q21.31 deletions: broadening the clinical spectrum and genotype-phenotype correlations in a large cohort of patients

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Description scientific article published on 30 September 2015
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author: Eugenio Mercuri  Ilaria Contaldo  Marni Falk  Anita Rauch 

Publication date September 30, 2015
Language English
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