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Results 51-60 of 5308 (Search time: 0.006 seconds).
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PreviewIssue DateTitleAuthor(s)
2003Frequency of major molecular responses to imatinib or interferon alfa plus cytarabine in newly diagnosed chronic myeloid leukemiaHughes, T.; Kaeda, J.; Branford, S.; Rudzki, Z.; Hochhaus, A.; Hensley, M.; Gathmann, I.; Bolton, A.; van Hoomissen, I.; Goldman, J.; Radich, J.
20041024C>T (R342X) is a recurrent RHF6 mutation also found in the original Börjeson-Forssman-Lehmann syndrome familyLower, K.; Solders, G.; Bondeson, M.; Nelson, J.; Brun, A.; Crawford, J.; Malm, G.; Borjeson, M.; Turner, G.; Partington, M.; Gecz, J.
2011The power of one and its costNorman, R.
1998Molecular heterogeneity in mucopolysaccharidosis IVA in Australia and Northern Ireland: nine novel mutations including T312S, a common allele that confers a mild phenotypeYamada, N.; Fukuda, S.; Tomatsu, S.; Muller, V.; Hopwood, J.; Nelson, J.; Kato, Z.; Yamagishi, A.; Sukegawa, K.; Kondo, M.; Orii, T.
2012Associations between resident perceptions of the local residential environment and metabolic syndromeBaldock, K.; Paquet, C.; Howard, N.; Coffee, N.; Hugo, G.; Taylor, A.; Adams, R.; Daniel, M.
2004Binners, fillers and filers - a qualitative study of GPs who don't return postal questionnairesStocks, N.; Braunack-Mayer, A.; Somerset, M.; Gunnell, D.
2012The use of negative themes in television food advertisingPettigrew, S.; Roberts, M.; Chapman, K.; Quester, P.; Miller, C.
2012Broadening the phenotype associated with mutations in UPF3B: two further cases with renal dysplasia and variable developmental delayLynch, S.; Nguyen, L.; Ng, L.; Waldron, M.; McDonald, D.; Gecz, J.
2004Pseudo-fascicular activity originating from the right ventricular outflow tractTakahashi, Y.; Sanders, P.; Ho, S.; Haissaguerre, M.
2010Does access to compensation have an impact on recovery outcomes after injury?O'Donnell, M.; Creamer, M.; McFarlane, A.; Silove, D.; Bryant, R.