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FBXO28 is a critical gene of the 1q41q42 microdeletion syndrome
Author(s) -
Cassina Matteo,
Rigon Chiara,
Casarin Alberto,
Vicenzi Virginia,
Salviati Leonardo,
Clementi Maurizio
Publication year - 2015
Publication title -
american journal of medical genetics part a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.064
H-Index - 112
eISSN - 1552-4833
pISSN - 1552-4825
DOI - 10.1002/ajmg.a.37033
Subject(s) - medical genetics , unit (ring theory) , medicine , pediatrics , family medicine , library science , psychology , genetics , biology , gene , computer science , mathematics education
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