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PreviewIssue DateTitleAuthor(s)
1997Mapping of the gene for vascular endothelial growth factor-D in mouse and man to the X chromosomeJenkins, N.; Woollatt, E.; Crawford, J.; Gilbert, D.; Baldwin, M.; Sutherland, G.; Copeland, N.; Achen, M.
1995Exposure to environmental lead and visual motor integration at 7 years: The Port Pirie Cohort StudyBaghurst, P.; McMichael, A.; Tong, S.; Wigg, N.; Vimpani, G.; Robertson, E.
1996Children with hyperimmunoglobulinemia D and periodic fever syndromeGrose, C.; Schnetzer, J.; Ferrante, A.; Vladutiu, A.
1995Mechanisms of small ring formation suggested by the molecular characterization of 2 small accessory ring chromosomes derived from chromosome 4Fang, Y.; Eyre, H.; Bohlander, S.; Estop, A.; McPherson, E.; Trager, T.; Riess, O.; Callen, D.
1998Coexistence of Gaucher-Disease Type 1 and Joubert-SyndromeVan Royen-Kerkhof, A.; Pollthe, B.; Kleijer, W.; van Diggelen, O.; Aerts, J.; Hopwood, J.; Beemer, F.
2007The mental health and wellbeing of children and adolescents in home-based foster careSawyer, M.; Carbone, J.; Searle, A.; Robinson, P.
2003MJA Practice Essentials - 2: Recent advances in therapy of diabetes - EndocrinologyCouper, J.; Prins, J.
2003Two further cases of Ohdo syndrome delineate the phenotypic variability of the conditionWhite, S.; Ades, L.; Amor, D.; Liebelt, J.; Bankier, A.; Baker, E.; Wilson, M.; Savarirayan, R.
2008Effect of long-chain polyunsaturated fatty acid supplementation of preterm infants on disease risk and neurodevelopment: a systematic review of randomized controlled trialsSmithers, L.; Gibson, R.; McPhee, A.; Makrides, M.
2008X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairmentDibbens, L.; Tarpey, P.; Hynes, K.; Bayly, M.; Scheffer, I.; Smith, R.; Bomar, J.; Sutton, E.; Vandeleur, L.; Shoubridge, C.; Edkins, S.; Turner, S.; Stevens, C.; O'Meara, S.; Tofts, C.; Barthorpe, S.; Buck, G.; Cole, J.; Halliday, K.; Jones, D.; et al.