Adelaide Research & Scholarship: Search

Search

Results 1-5 of 5 (Search time: 0.002 seconds).

previous
1
next

Item hits:

Preview	Issue Date	Title	Author(s)
	2001	Loss of heterozygosity mapping at chromosome arm 16q in 712 breast tumors reveals factors that influence delineation of candidate regions	Cleton-Jansen, A.; Callen, D.; Seshadri, R.; Goldup, S.; McCallum, B.; Crawford, J.; Powell, J.; Settasatian, C.; van Beerendonk, H.; Moerland, E.; Smit, V.; Harris, W.; Millis, R.; Morgan, N.; Barnes, D.; Mathew, C.; Cornelisse, C.
	2001	A novel Q378X mutation exists in the transmembrane transporter protein ABCC6 and its pseudogene: implications for mutation analysis in pseudoxanthoma elasticum	Cai, L.; Lumsden, A.; Guenther, U.; Nelder, S.; Zach, S.; Knoblauch, H.; Ramesar, R.; Hohl, D.; Callen, D.; Neldner, K.; Lindpaintner, K.; Richards, R.; Struk, B.
	2001	Karyotypes found in the population declared at increased risk of Down Syndrome following maternal serum screening	Ryall, R.; Callen, D.; Cocciolone, R.; Duvnjak, A.; Esca, R.; Frantzis, N.; Gjerde, E.; Haan, E.; Hocking, T.; Sutherland, G.; Thomas, D.; Webb, F.
	2001	Analysis of lymphoedema-distichiasis families for FOXC2 mutations reveals small insertions and deletions throughout the gene	Bell, R.; Brice, G.; Child, A.; Murday, V.; Mansour, S.; Sandy, C.; Collin, J.; Brady, A.; Callen, D.; Burnand, K.; Mortimer, P.; Jeffery, S.
	2001	Molecular and functional analyses of the human and mouse genes encoding AFG3L1, a mitochondrial metalloprotease homologous to the human spastic paraplegia protein	Kremmidiotis, G.; Gardner, A.; Settasatian, C.; Savoia, A.; Sutherland, G.; Callen, D.