E-mail

E-mail a Wiley Online Library Link

Göran Carlsson, Göran Elinder, Helena Malmgren, Alicja Trebinska, Ewa Grzybowska, Niklas Dahl, Magnus Nordenskjöld and Bengt Fadeel Compound heterozygous HAX1 mutations in a Swedish patient with severe congenital neutropenia and no neurodevelopmental abnormalities Pediatric Blood & Cancer 53

Article first published online: 4 JUN 2009 | DOI: 10.1002/pbc.22131

Complete the form below and we will send an e-mail message containing a link to the selected article on your behalf

Required = Required Field

Choose captcha format: Image or Audio. Click here if you need help.

SEARCH