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Results 31-40 of 584 (Search time: 0.003 seconds).
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PreviewIssue DateTitleAuthor(s)
2007Epidemiological comparisons of problems and positive qualities reported by adolescents in 24 countriesRescorla, L.; Achenbach, T.; Ivanova, M.; Dumenci, L.; Almqvist, F.; Bilenberg, N.; Bird, H.; Broberg, A.; Dobrean, A.; Dopfner, M.; Erol, N.; Forns, M.; Hannesdottir, H.; Kanbayashi, Y.; Lambert, M.; Leung, P.; Minaei, A.; Mulatu, M.; Novik, T.; Oh, K.; et al.
2002Pancreatic disorders and cystic fibrosis: Working Group Report of the First World Congress of Pediatric Gastroenterology, Hepatology, and NutritionCouper, R.; Belli, D.; Durie, P.; Gaskin, K.; Sarles, J.; Werlin, S.
2004TM4SF10 gene sequencing in XLMR patients identifies common polymorphisms but no disease-associated mutationChristophe-Hobertus, C.; Kooy, F.; Gecz, J.; Abramowicz, M.; Holinski-Feder, E.; Schwartz, C.; Christophe, D.
2002A complex rearrangement involving simultaneous translocation and inversion is associated with a change in chromatin compactionCallen, D.; Eyre, H.; McDonnell, S.; Schuffenhauer, S.; Bhalla, K.
2008A novel locus for X-linked congenital cataract on Xq24Craig, J.; Friend, K.; Gecz, J.; Rattray, K.; Trotski, M.; Mackey, D.; Burdon, K.
2002Results of consecutive trials for children newly diagnosed with acute myeloid leukemia from the Australian and New Zealand Children's Cancer Study GroupO'Brien, T.; Russell, S.; Vowels, M.; Oswald, C.; Tiedemann, K.; Shaw, P.; Lockwood, L.; Teague, L.; Rice, M.; Marshall, G.
2008Current use of Australian snake antivenoms and frequency of immediate-type hypersensitivity reactions and anaphylaxisIsbister, G.; Brown, S.; MacDonald, E.; White, J.; Currie, B.
2008Novel causative mutations in patients with Nance-Horan syndrome and altered localization of the mutant NHS-A protein isoformSharma, S.; Burdon, K.; Dave, A.; Jamieson, R.; Yaron, Y.; Billson, F.; van Maldergem, L.; Lorenz, B.; Gecz, J.; Craig, J.
2001A single nucleotide polymorphism in the 5' untranslated region of RAD51 and risk of cancer among BRCA1/2 mutation carriersWang, W.; Spurdle, A.; Kolachana, P.; Bove, B.; Modan, B.; Ebbers, S.; Suthers, G.; Tucker, M.; Kaufman, D.; Doody, M.; Tarone, R.; Daly, M.; Levavi, H.; Pierce, H.; Chetrit, A.; Yechezkel, G.; Chenevix-Trench, G.; Offit, K.; Godwin, A.; Struewing, J.
2000New mutations in MID1 provide support for loss of function as the cause of X-linked Optiz syndromeCox, T.; Allen, L.; Cox, L.; Hopwood, B.; Goodwin, B.; Haan, E.; Suthers, G.

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