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Results 21-30 of 95 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
1997Unbalanced t(4;11)(q32-q23) in a 34-year-old man with manifestations of distal monosomy 11q and trisomy 4q syndromesByatt, S.; Baker, E.; Richards, R.; Roberts, C.; Smith, A.
1995Bladder, urethral and vaginal duplication: a case report.Goh, D.; Davey, R.; Dewan, P.
1999Chronic recurrent multifocal osteomyelitis associated with chronic inflammatory bowel disease in childrenBousvaros, A.; Marcon, M.; Treem, W.; Waters, P.; Issenman, R.; Couper, R.; Burnell, R.; Rosenberg, A.; Rabinovich, E.; Kirschner, B.
1998Identification of a common mutation (R245h) in Sanfilippo A patients from the NetherlandsWeber, B.; Vandekamp, J.; Kleijer, W.; Guo, X.H.; Blanch, L.; van Diggelen, O.; Wevers, R.; Poorthuis, B.; Hopwood, J.
1997Randomized, comparative trial of 20 micrograms vs 40 micrograms Engerix B vaccine in hepatitis B vaccine non-respondersGoldwater, P.
1995Immunoglobulin M capture immunoassay in investigation of coxsackie B5 and B6 outbreaks in South AustraliaGoldwater, P.
1999The autonomic control of heart rate and insulin resistance in young adultsFlanagan, D.; Vaile, J.; Petley, G.; Moore, V.; Godsland, I.; Cockington, R.; Robinson, J.; Phillips, D.
1996FRAGILE X SYNDROME AND FRAGILE XE MENTAL RETARDATION [Review]Sutherland, G.; Mulley, J.
1996Clinicopathologic features of congenital aneurysms of the great vesselsAdes, L.; Knight, W.; Byard, R.; Bateman, J.; Esquivel, J.; Mee, R.; Haan, E.; Milewicz, D.
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.