Next-Generation Sequencing Reveals A JAGN1 Mutation in a Syndromic Child with Intermittent Neutropenia

MLA

Giuseppe Palumbo, et al. Next-Generation Sequencing Reveals A JAGN1 Mutation in a Syndromic Child with Intermittent Neutropenia. Jan. 2018. EBSCOhost, widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsair&AN=edsair.doi.dedup.....051a806d50bcb10ae7c4a0aae46ecb53&authtype=sso&custid=ns315887.

APA

Giuseppe Palumbo, Gigliola Di Matteo, Caterina Cancrini, Rita De Vito, Immacolata Brigida, Cristina Cifaldi, Jessica Serafinelli, Paolo Rossi, Alessandro Aiuti, Paolo Palma, Silvia Di Cesare, Andrea Finocchi, Davide Petricone, & Maria Chiriaco. (2018). Next-Generation Sequencing Reveals A JAGN1 Mutation in a Syndromic Child with Intermittent Neutropenia.

Chicago

Giuseppe Palumbo, Gigliola Di Matteo, Caterina Cancrini, Rita De Vito, Immacolata Brigida, Cristina Cifaldi, Jessica Serafinelli, et al. 2018. “Next-Generation Sequencing Reveals A JAGN1 Mutation in a Syndromic Child with Intermittent Neutropenia,” January. http://widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsair&AN=edsair.doi.dedup.....051a806d50bcb10ae7c4a0aae46ecb53&authtype=sso&custid=ns315887.