Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease von Snell, Russell G, MacMillan, John C, Cheadle, Jeremy P, Fenton, Iain, Lazarou, Lazarus P, Davies, Peter, MacDonald, Marcy E, Gusella, James F, Harper, Peter S, Shaw, Duncan J

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Huntington Disease: Who Seeks Presymptomatic Genetic Testing, Why and What are the Outcomes? von Scuffham, Tracey M., MacMillan, John C.

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PAK3 mutation in nonsyndromic X-linked mental retardation von Walsh, Christopher A, Allen, Kristina M, Gleeson, Joseph G, Bagrodia, Shubha, Partington, Michael W, MacMillan, John C, Cerione, Richard A, Mulley, John C

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DHPLC mutation analysis of Jagged1 (JAG1) reveals six novel mutations in Australian alagille syndrome patients von Heritage, Mandy L., MacMillan, John C., Anderson, Gregory J.

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An investigation of the 5-HT2C receptor gene as a migraine candidate gene von Johnson, Matthew P., Lea, Rod A., Curtain, Robert P., MacMillan, John C., Griffiths, Lyn R.

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Jagged1 (JAG1) mutation detection in an Australian Alagille syndrome population von Heritage, Mandy L., MacMillan, John C., Colliton, Raymond P., Genin, Anna, Spinner, Nancy B., Anderson, Gregory J.

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Clinical and genetic study of Friedreich ataxia in an Australian population von Delatycki, Martin B., Paris, Damien B.B.P., Gardner, R.J. McKinlay, Nicholson, Garth A., Nassif, Najah, Storey, Elsdon, MacMillan, John C., Collins, Veronica, Williamson, Robert, Forrest, Susan M.

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The early history of the Catholic Church in Prince Edward Island / by John C. Macmillan von Macmillan, John C

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The early history of the Catholic Church in Prince Edward Island / by John C. Macmillan von Macmillan, John C

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The history of the Catholic church in Prince Edward Island, from 1835 till 1891 / by John C. Macmillan von Macmillan, John C

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Size of the unstable CTG repeat sequence in relation to phenotype and parental transmission in myotonic dystrophy von HARLEY, H. G, RUNDLE, S. A, MACMILLAN, J. C, MYRING, J, BROOK, J. D, CROW, S, REARDON, W, FENTON, I, SHAW, D. J, HARPER, P. S

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Partial Characterisation of Murine Huntingtin and Apparent Variations in the Subcellular Localisation of Huntingtin in Human, Mouse and Rat Brain von Wood, Jonathan D., MacMillan, John C., Harper, Peter S., Lowenstein, Pedro R., Jones, A. Lesley

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DHPLC mutation analysis ofJagged1 (JAG1) reveals six novel mutations in Australian alagille syndrome patients von Heritage, Mandy L., MacMillan, John C., Anderson, Gregory J.

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An investigation of the 5‐HT 2C receptor gene as a migraine candidate gene von Johnson, Matthew P., Lea, Rod A., Curtain, Robert P., MacMillan, John C., Griffiths, Lyn R.

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Outpatient costing and classification von MacMillan, John C, Barlow, Megan, Cloherty, Jim

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5 Arteriohepatic dysplasia (Alagille syndrome; Watson-Alagille syndrome) von MacMillan, John C., Shepherd, Ross, Heritage, Mandy

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Arteriohepatic dysplasia (Alagille syndrome; Watson-Alagille syndrome) von MacMillan, J C, Shepherd, R, Heritage, M

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Functional Neural Transplantation von Macmillan, John C

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Genome Maps and Neurological Disorders von Macmillan, John C

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The Molecular and Genetic Basis of Neurological Disease von Macmillan, John C

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