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Current Opinion in Neurology|March 23, 2001
Molecular genetics of human microcephalyG H Mochida, C A WalshJournal of Medical Genetics|September 6, 2005
ASPM mutations identified in patients with primary microcephaly and seizuresJ Shen, W Eyaid, G H Mochida, et al.Neurology|May 29, 2003
A novel form of pontocerebellar hypoplasia maps to chromosome 7q11-21A Rajab, G H Mochida, A Hill, et al.Human Molecular Genetics|September 5, 2001
Mutations in the X-linked filamin 1 gene cause periventricular nodular heterotopia in males as well as in femalesV L Sheen, P H Dixon, J W Fox, et al.Pageof 1