Functional rescue of mutant ABCA1 proteins by sodium 4-phenylbutyrate[S] von Sorrenson, Brie, Suetani, Rachel J., Williams, Michael J.A., Bickley, Vivienne M., George, Peter M., Jones, Gregory T., McCormick, Sally P.A.

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Copy number variants implicate cardiac function and development pathways in earthquake-induced stress cardiomyopathy von Lacey, Cameron J., Doudney, Kit, Bridgman, Paul G., George, Peter M., Mulder, Roger T., Zarifeh, Julie J., Kimber, Bridget, Cadzow, Murray J., Black, Michael A., Merriman, Tony R., Lehnert, Klaus, Bickley, Vivienne M, Pearson, John F., Cameron, Vicky A., Kennedy, Martin A.

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NRAS and EPHB6 mutation rates differ in metastatic melanomas of patients in the North Island versus South Island of New Zealand von Jones, Angela M, Ferguson, Peter, Gardner, Jacqui, Rooker, Serena, Sutton, Tim, Ahn, Antonio, Chatterjee, Aniruddha, Bickley, Vivienne M, Sarwar, Makhdoom, Emanuel, Patrick, Kenwright, Diane, Shepherd, Peter R, Eccles, Michael R

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Trilateral Retinoblastoma in a Patient With Peutz-Jeghers Syndrome von Raizis, Anthony M., Van Mater, David, Aaltonen, Lauri A., Lohmann, Dietmar, Cheale, Michelle S., Bickley, Vivienne M., George, Peter M., Zhou, Yaolin, Rosoff, Philip M.

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An ABCA1 truncation shows no dominant negative effect in a familial hypoalphalipoproteinemia pedigree with three ABCA1 mutations von Sorrenson, Brie, Suetani, Rachel J., Bickley, Vivienne M., George, Peter M., Williams, Michael J.A., Scott, Russell S., McCormick, Sally P.A.

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Rare Complete and Partial Monosomy 7 Mosaicism Detected in a Case with FTT and Borderline Motor Delay, Subsequently Diagnosed with Juvenile MDS: An Exposition of this Case and Othe... von Bickley, Vivienne M, Parker, Elsa M, Taylor, Jill C, Watt, Jane E, Robertson, Monique D, Doudney, Kit W.E, Cross, Siobhan, Townsend, Janine, Kidd, Alexa M.J, George, Peter M

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Trilateral Retinoblastoma in a Patient With Peutz– J eghers Syndrome von Raizis, Anthony M., Van Mater, David, Aaltonen, Lauri A., Lohmann, Dietmar, Cheale, Michelle S., Bickley, Vivienne M., George, Peter M., Zhou, Yaolin, Rosoff, Philip M.

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Fatty infiltration of the liver in a case of hypobetalipoproteinaemia with a novel mutation in the APOB gene von Florkowski, C. M

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