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Delineation of the clinical profile of <i>CNOT2</i> haploinsufficiency and overview of the IDNADFS phenotype

Marcello Niceta et al.
HAL (France) · Papers · License: Open Access
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IDNADFS, 1, CNOTs-related disorders, CNOT2mutations, 2, 0, 12q15microdeletionsyndrome
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Record · ID 274346
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