Compound heterozygote CDK5RAP2 mutations in a Guatemalan/Honduran child with autosomal recessive primary microcephaly, failure to thrive and speech delay. (21st April 2015) - Li, Mindy H; Arndt, Kelly; Das, Soma; Weiss, Elliott M; Wu, Yaning; Gwal, Kriti; Shekdar, Karuna V; Zackai, Elaine H