Variants in ACTG2 underlie a substantial number of Australasian patients with primary chronic intestinal pseudo‐obstruction von Ravenscroft, G., Pannell, S., O'Grady, G., Ong, R., Ee, H. C., Faiz, F., Marns, L., Goel, H., Kumarasinghe, P., Sollis, E., Sivadorai, P., Wilson, M., Magoffin, A., Nightingale, S., Freckmann, M.‐L., Kirk, E. P., Sachdev, R., Lemberg, D. A., Delatycki, M. B., Kamm, M. A., Basnayake, C., Lamont, P. J., Amor, D. J., Jones, K., Schilperoort, J., Davis, M. R., Laing, N. G.

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Variants in ACTG 2 underlie a substantial number of Australasian patients with primary chronic intestinal pseudo‐obstruction von Ravenscroft, G., Pannell, S., O'Grady, G., Ong, R., Ee, H. C., Faiz, F., Marns, L., Goel, H., Kumarasinghe, P., Sollis, E., Sivadorai, P., Wilson, M., Magoffin, A., Nightingale, S., Freckmann, M.‐L., Kirk, E. P., Sachdev, R., Lemberg, D. A., Delatycki, M. B., Kamm, M. A., Basnayake, C., Lamont, P. J., Amor, D. J., Jones, K., Schilperoort, J., Davis, M. R., Laing, N. G.

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Leigh disease caused by the mitochondrial DNA G14459A mutation in unrelated families von Kirby, Denise M., Kahler, Stephen G., Freckmann, Mary-Louise, Reddihough, Dinah, Thorburn, David R.

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Infantile Spasms Is Associated with Deletion of the MAGl2 Gene on Chromosome 7q11.23-q21.11 von Marshail, C R, Young, E J, Pani, A M, Freckmann, M-L, Lacassle, Y, Howald, C, Fitzgerald, K K, Peippo, M, Morris, CA, Shane, K, Priolo, M, Morimoto, M, Kondo, I, Osborne, L R

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Naevus of Ota presenting in two generations: a mother and daughter von Agero, A L C, Lahmar, J J, Holzborn, R M, Martin, L K, Freckmann, M-L, Murrell, D F

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