We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleIntragenic deletions and duplications of the LIS1 and DCX genes: a major disease-causing mechanism in lissencephaly and subcortical band heterotopia.AuthorsHaverfield EV; Whited AJ; Petras KS; Dobyns WB; Das SPublicationEuropean journal of human genetics : EJHG, 2009, Vol 17, Issue 7, p911ISSN1476-5438Publication typearticleDOI10.1038/ejhg.2008.213