Mutations in filamin 1 prevent migration of cerebral cortical neurons in human periventricular heterotopia

• Fox JW, Lamperti ED, Eksioglu YZ, Hong SE, Feng Y, Graham DA, Scheffer IE, Dobyns WB, Hirsch BA, Radtke RA, Berkovic SF, Huttenlocher PR, Walsh CA

• Neuron. 1998 21(6): 1315-1325

• [Abstract] | [PubMed Link] | [Full Text]

PAK3 mutation in nonsyndromic X-linked mental retardation

• Allen KM, Gleeson JG, Bagrodia S, Partington MW, MacMillan JC, Cerione RA, Mulley JC, Walsh CA

• Nature Genetics. 1998 20(1): 25-30

• [Abstract] | [PubMed Link]

LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation

• Pilz DT, Matsumoto N, Minnerath S, Mills P, Gleeson JG, Allen KM, Walsh CA, Barkovich AJ, Dobyns WB, Ledbetter DH, Ross ME

• Human Molecular Genetics. 1998 Dec;7(13):2029-37

• [PubMed Link]

A YAC contig in Xq23, from DXS287 to DXS2088, spanning the critical region for double cortex/X-linked lissencephaly (DC/XLIS)