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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1949 1
1950 2
1970 1
1976 1
1978 2
1979 1
1981 1
1986 2
1987 1
1989 1
1991 1
1992 3
1993 7
1994 3
1995 2
1996 2
1997 1
1998 3
1999 3
2000 1
2001 3
2002 1
2003 2
2004 1
2005 2
2010 2
2011 2
2012 1
2014 1
2023 0
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Search Results

52 results
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Page 1
Clinical genetics in neurological disease.
MacMillan JC, Harper PS. MacMillan JC, et al. J Neurol Neurosurg Psychiatry. 1994 Jan;57(1):7-15. doi: 10.1136/jnnp.57.1.7. J Neurol Neurosurg Psychiatry. 1994. PMID: 8301308 Free PMC article. Review. No abstract available.
Outpatient costing and classification.
MacMillan JC, Barlow M, Cloherty J. MacMillan JC, et al. Med J Aust. 1999 Mar 15;170(6):286-7. doi: 10.5694/j.1326-5377.1999.tb127771.x. Med J Aust. 1999. PMID: 10212660 No abstract available.
Dentatorubral and pallidoluysian atrophy (DRPLA). Clinical and neuropathological findings in genetically confirmed North American and European pedigrees.
Becher MW, Rubinsztein DC, Leggo J, Wagster MV, Stine OC, Ranen NG, Franz ML, Abbott MH, Sherr M, MacMillan JC, Barron L, Porteous M, Harper PS, Ross CA. Becher MW, et al. Among authors: macmillan jc. Mov Disord. 1997 Jul;12(4):519-30. doi: 10.1002/mds.870120408. Mov Disord. 1997. PMID: 9251070 Review.
PAK3 mutation in nonsyndromic X-linked mental retardation.
Allen KM, Gleeson JG, Bagrodia S, Partington MW, MacMillan JC, Cerione RA, Mulley JC, Walsh CA. Allen KM, et al. Among authors: macmillan jc. Nat Genet. 1998 Sep;20(1):25-30. doi: 10.1038/1675. Nat Genet. 1998. PMID: 9731525
Characterising the Huntington's disease gene product.
Wood J, MacMillan JC, Thomas P, Lowenstein PR, Harper PS, Jones AL. Wood J, et al. Among authors: macmillan jc. Biochem Soc Trans. 1995 Nov;23(4):595S. doi: 10.1042/bst023595s. Biochem Soc Trans. 1995. PMID: 8654780 No abstract available.
52 results