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Genetic evidence for a distinct subtype of schizophrenia characterized by pervasive cognitive deficit

- Hallmayer, J.F., Badcock, J., Dragovi, M., Howell, S., Michie, Patricia Therese, Rock, D., Vile, D., Williams, R., Jablensky, A., Kalaydjieva, L., Hollingsworth, K., Corder, E.H.

Mutation analysis of the MYH gene in an Australian series of colorectal polyposis patients with or without germline APC mutations

- Kairupan, Carla F., Meldrum, C. J., Crooks, R., Milward, E. A., Spigelman, Allan David, Burgess, B., Groombridge, C., Kirk, J., Tucker, K., Ward, R., Williams, R., Scott, Rodney J

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