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Preview	Issue Date	Title	Author(s)
	2014	Prediction of potential cancer-risk regions based on transcriptome data: towards a comprehensive view	Alisoltani, A.; Fallahi, H.; Ebrahimi, M.; Ebrahimi, M.; Ebrahimie, E.; Coleman, W.
	2003	The clinical geneticist and the "new genetics"	Haan, E.
	2021	Of 'junk food' and 'brain food': how parental diet influences offspring neurobiology and behaviour	Bodden, C.; Hannan, A.J.; Reichelt, A.C.
	2019	GJB2 and GJB6 mutations in hereditary recessive non-syndromic hearing impairment in Cameroon	Tingang Wonkam, E.; Chimusa, E.; Noubiap, J.J.; Adadey, S.M.; F Fokouo, J.V.; Wonkam, A.
	1996	A novel mutation in Exon 6 (F236S) of the proteolipid protein gene is associated with spastic paraplegia	Donnelly, A.; Colley, A.; Crimmins, D.; Mulley, J.
	2019	The impact of genetic adaptation on chimpanzee subspecies differentiation	Schmidt, J.M.; de Manuel, M.; Marques-Bonet, T.; Castellano, S.; Andrés, A.M.; Gojobori, T.
	2021	HYPOXIA AND REPRODUCTIVE HEALTH: hypoxia and ovarian function: follicle development, ovulation, oocyte maturation	Lim, M.; Thompson, J.G.; Dunning, K.R.
	1996	How many X-linked genes for non-specific mental retardation (MRX) are there?	Gedeon, A.; Donnelly, A.; Mulley, J.; Kerr, B.; Turner, G.
	1998	Febrile seizures and generalised epilepsy associated with a mutation in the Na+-channel b1 subunit gene SCN1B	Wallace, R.; Wang, D.; Singh, R.; Scheffer, I.; George Jnr., A.; Phillips, H.; Saar, K.; Reis, A.; Johnson, E.; Sutherland, G.; Berkovic, S.; Mulley, J.
	1995	X linked fatal infantile cardiomyopathy maps to Xq28 and is possibly allelic to Barth syndrome	Gedeon, A.; Wilson, M.; Colley, A.; Sillence, D.; Mulley, J.