A heterozygous, intragenic deletion of CNOT2 recapitulates the phenotype of 12q15 deletion syndrome
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| Description | scientific article published on 30 May 2019 |
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author: Antonio Novelli Fabrizio Drago Anwar Baban Silvia Genovese Valeria Orlando Viola Alesi Sara Loddo |
| Publication date | May 30, 2019 |
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