Adelaide Research & Scholarship: Search

Search

Results 41-50 of 89 (Search time: 0.003 seconds).

previous
1
...
2
3
4
5
6
7
8
...
9
next

Item hits:

Preview	Issue Date	Title	Author(s)
	2001	Long-term outcomes of genetic counseling in women at increased risk of developing hereditary breast cancer	Meiser, B.; Butow, P.; Barratt, A.; Schneiden, V.; Gattas, M.; Kirk, J.; Gaff, C.; Suthers, G.; Tucker, K.
	2007	An absence of cutaneous neurofibromas associated with a 3-bp inframe deletion in Exon 17 of the NF1 gene (c.2970-2972 delAAT): evidence of a clinically significant NF1 genotype-phenotype correlation	Upadyaya, M.; Huson, S.; Davies, M.; Thomas, N.; Chuzhanova, N.; Giovannini, S.; Evans, D.; Howard, E.; Kerr, B.; Kerr, B.; Consoli, C.; Side, L.; Adams, D.; Pierpont, M.; Hatchen, R.; Barnicoat, A.; Li, H.; Wallace, P.; Van Biervliet, J.; Stevenson, D.; et al.
	2001	A recurrent RNA-splicing mutation in the SEDL gene causes X-linked spondyloepiphyseal dysplasia tarda	Tiller, G.; Hannig, V.; Dozier, D.; Carrel, L.; Trevarthen, K.; Wilcox, W.; Mundlos, S.; Haines, J.; Gedeon, A.; Gecz, J.
	2002	National study of adverse reactions after vaccination with bacille Calmette-Guérin	Turnbull, F.; McIntyre, P.; Achat, H.; Wang, H.; Stapledon, R.; Gold, M.; Burgess, M.
	2004	Nasopharyngeal pH monitoring in chronic sinusitis patients using a novel four channel probe	Wong, I.; Omari, T.; Myers, J.; Rees, G.; Nair, S.; Jamieson, G.; Wormald, P.
	2007	Functional characterization of GATA3 mutations causing the hypoparathyroidism-deafness-renal (HDR) dysplasia syndrome: insight into mechanisms of DNA binding by the GATA3 transcription factor	Ali, A.; Christie, P.; Grigorieva, I.; Harding, B.; Van Esch, H.; Ahmed, S.; Bitner-Glindzicz, M.; Blind, E.; Bloch, C.; Christin, P.; Clayton, P.; Gecz, J.; Gilbert-Dussardier, B.; Guillen-Navarro, E.; Hackett, A.; Halac, I.; Hendy, G.; Lalloo, F.; Mache, C.; Mughal, Z.; et al.
	2005	Increased intracellular pro- and anti-inflammatory cytokines in bronchoalveolar lavage T cells of stable lung transplant patients	Hodge, G.; Hodge, S.; Reynolds, P.; Holmes, M.
	2009	Sporadic in utero generalized edema caused by mutations in the lymphangiogenic genes VEGFR3 and FOXC2	Ghalamkarpour, A.; Debauche, C.; Haan, E.; Van Regemorter, N.; Snzajer, Y.; Thomas, D.; Revencu, N.; Gillerot, Y.; Boon, L.; Vikkula, M.
	2009	Importance of background rates of disease in assessment of vaccine safety during mass immunisation with pandemic H1N1 influenza vaccines	Black, S.; Eskola, J.; Siegrist, C.; Halsey, N.; MacDonald, N.; Law, B.; Miller, E.; Andrews, N.; Stowe, J.; Salmon, D.; Vannice, K.; Izurieta, H.; Akhtar, A.; Gold, M.; Oselka, G.; Zuber, P.; Pfeifer, D.; Vellozi, C.
	2008	Baby Friendly Hospital Initiative practices and breast feeding duration in a cohort of first-time mothers in Adelaide, Australia	Pincombe, J.; Baghurst, P.; Antonjou, G.; Peat, B.; Henderson, A.; Reddin, E.