DSpace at RU >

Browsing by Author Wilson, M.

Full Text	Issue Date	Title	Author(s)
	2010	The 2q23.1 microdeletion syndrome: clinical and behavioural phenotype.	Bon, B.W.M. van; Koolen, D.A.; Brueton, L., et al
	2009	The area centralis in the chicken retina contains efferent target amacrine cells.	Weller, C.; Lindstrom, S.H.; Grip, W.J. de, et al
	2011	An Australian tuberous sclerosis cohort: are surveillance guidelines being met?	Chopra, M.; Lawson, J.A.; Wilson, M., et al
	2009	Breast cancer risk is not increased in individuals with TWIST1 mutation confirmed Saethre-Chotzen syndrome: an Australian multicenter study.	James, P.A.; Culling, B.; Mullan, G., et al
	2010	Cardiovascular function and the veteran athlete.	Wilson, M.; O'Hanlon, R.; Basavarajaiah, S., et al
	2010	Ex-vivo HRMAS of adult brain tumours: metabolite quantification and assignment of tumour biomarkers.	Wright, A.J.; Fellows, G.A.; Griffiths, J.R., et al
	2009	Further clinical and molecular delineation of the 9q subtelomeric deletion syndrome supports a major contribution of EHMT1 haploinsufficiency to the core phenotype.	Kleefstra, T.; Zelst-Stams, W.A. van; Nillesen, W.M., et al
	2010	Genome-wide profiling of p63 DNA-binding sites identifies an element that regulates gene expression during limb development in the 7q21 SHFM1 locus.	Kouwenhoven, E.N.; Heeringen, S.J. van; Tena, J.J., et al
	2008	Visually assessed breast density, breast cancer risk and the importance of the craniocaudal view.	Duffy, S.W.; Nagtegaal, I.D.; Astley, S.M., et al