Zobrazeno 1 - 10
of 26
pro vyhledávání: '"McKinlay Gardner, R. J"'
Autor:
Nickerson, Sarah L., Marquis-Nicholson, Renate, Claxton, Karen, Ashton, Fern, Leong, Ivone U. S., Prosser, Debra O., Love, Jennifer M., George, Alice M., Taylor, Graham, Wilson, Callum, McKinlay Gardner, R. J., Love, Donald R.
Publikováno v:
Microarrays (2076-3905); 2015, Vol. 4 Issue 4, p490-502, 13p
Publikováno v:
Prenatal Diagnosis; Apr2012, Vol. 32 Issue 4, p389-395, 7p
Autor:
Andreucci, Elena, Aftimos, Salim, Alcausin, Melanie, Haan, Eric, Hunter, Warwick, Kannu, Peter, Kerr, Bronwyn, McGillivray, George, McKinlay Gardner, R J, Patricelli, Maria G, Sillence, David, Thompson, Elizabeth, Zacharin, Margaret, Zankl, Andreas, Lamandé, Shireen R, Savarirayan, Ravi
Publikováno v:
Orphanet Journal of Rare Diseases; 2011, Vol. 6 Issue 1, p37-44, 8p
Autor:
McKinlay Gardner, R. J., Knight, Melanie A., Hara, Kenju, Tsuji, Shoji, Forrest, Susan M., Storey, Elsdon
Publikováno v:
Cerebellum; Mar2005, Vol. 4 Issue 1, p47-50, 4p
Autor:
Singh, Rita, McKinlay Gardner, R. J, Crossland, Kathryn M, Scheffer, Ingrid E, Berkovic, Samuel F
Publikováno v:
Epilepsia (Series 4); Feb2002, Vol. 43 Issue 2, p127-140, 14p
Autor:
Lamandé, Shireen R., Bateman, John F., Hutchison, Wendy, McKinlay Gardner, R. J., Bower, Simon P., Byrne, Edward, Dahl, Hans‐Henrik M.
Publikováno v:
Human Molecular Genetics; Jun98, Vol. 7 Issue 6, p981, 9p
Dominantly inherited ataxia and dysphonia with dentate calcification: spinocerebellar ataxia type 20
Autor:
Knight, Melanie A., McKinlay Gardner, R. J., Bahlo, Melanie, Matsuura, Tohru, Dixon, Judith A., Forrest, Susan M., Storey, Elsdon
Publikováno v:
Brain: A Journal of Neurology; May, 2004, Vol. 127 Issue: 5 p1172-1181, 10p
Publikováno v:
Cerebellum; Mar2005, Vol. 4 Issue 1, p55-57, 3p
Autor:
Anita Vinton, Michael Fahey, Brien, Terence O., Shaw, Janet H., Elsdon Storey, Mckinlay Gardner, R. J., Mitchell, Peter J., Desiree Du Sart, King, John O.
Publikováno v:
Monash University
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::567f1f8e7ee765de71f34941e70a08c8
https://research.monash.edu/en/publications/fdb2f03f-aabb-4529-9391-5b39b4a6dc9b
https://research.monash.edu/en/publications/fdb2f03f-aabb-4529-9391-5b39b4a6dc9b
Autor:
Heliövaara E; Genome-Scale Biology Research Program, Department of Medical Genetics, University of Helsinki, 00014 Helsinki, Finland., Tuupanen S, Ahlsten M, Hodgson S, de Menis E, Kuismin O, Izatt L, McKinlay Gardner RJ, Gundogdu S, Lucassen A, Arola J, Tuomisto A, Mäkinen M, Karhu A, Aaltonen LA
Publikováno v:
Journal of molecular endocrinology [J Mol Endocrinol] 2010 Dec 21; Vol. 46 (1), pp. 1-8. Date of Electronic Publication: 2010 Dec 21 (Print Publication: 2011).