Published in
Wiley, The American Journal of Medical Genetics - Part A, 2019
DOI: 10.1002/ajmg.a.61217
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A heterozygous, intragenic deletion of CNOT2 recapitulates the phenotype of 12q15 deletion syndrome
Journal article published in 2019 by
Viola Alesi 
,
Sara Loddo ,
Federica Calì,
Valeria Orlando ,
Silvia Genovese ,
Daniele Ferretti,
Chiara Calacci,
Giusy Calvieri,
Roberto Falasca,
Lucia Ulgheri,
Fabrizio Drago,
Bruno Dallapiccola,
Anwar Baban ,
Antonio Novelli
,
Sara Loddo ,
Federica Calì,
Valeria Orlando ,
Silvia Genovese ,
Daniele Ferretti,
Chiara Calacci,
Giusy Calvieri,
Roberto Falasca,
Lucia Ulgheri,
Fabrizio Drago,
Bruno Dallapiccola,
Anwar Baban ,
Antonio Novelli
This paper is made freely available by the publisher.
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