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A Heterozygous, Intragenic Deletion of CNOT2 Recapitulates the Phenotype of 12q15 Deletion Syndrome

Viola Alesi,Sara Loddo,Federica Cali,Valeria Orlando,Silvia Genovese, Daniele Ferretti,Chiara Calacci,Giusy Calvieri,Roberto Falasca,Lucia Ulgheri,Fabrizio Drago,Bruno Dallapiccola,Anwar Baban,Antonio Novelli

American journal of medical genetics Part A（2019）

引用 11|浏览28
关键词
12q15,12q deletion syndrome,CNOT2
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