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American Journal of Human Genetics|August 13, 2011
Microcephaly with simplified gyration, epilepsy, and infantile diabetes linked to inappropriate apoptosis of neural progenitorsCathryn J Poulton, Rachel Schot, Sima Kheradmand Kia, et al.
American Journal of Human Genetics|September 4, 2012
RTTN mutations link primary cilia function to organization of the human cerebral cortexSima Kheradmand Kia, Elly Verbeek, Erik Engelen, et al.
European Journal of Human Genetics : EJHG|February 16, 2012
COL4A2 mutation associated with familial porencephaly and small-vessel diseaseElly Verbeek, Marije E C Meuwissen, Frans W Verheijen, et al.
American Journal of Medical Genetics. Part A|May 21, 2014
Severe presentation of WDR62 mutation: is there a role for modifying genetic factors?Cathryn J Poulton, Rachel Schot, Katja Seufert, et al.
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