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Results 1-10 of 31 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
2000Non-alcoholic steatohepatitis in children and adolescentsManton, N.; Lipsett, J.; Moore, D.; Davidson, G.; Bourne, A.; Couper, R.
2000Attitudes to genetic testing for breast cancer susceptibility in women at increased risk of developing hereditary breast cancerMeiser, B.; Butow, P.; Barratt, A.; Suthers, G.; Smith, M.; Colley, A.; Thompson, E.; Tucker, K.
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.
2000Intention to undergo prophylactic bilateral mastectomy in women at increased risk of developing hereditary breast cancerMeiser, B.; Butow, P.; Friedlander, M.; Schnieden, V.; Gattas, M.; Kirk, J.; Suthers, G.; Haan, E.; Tucker, K.
2000Treatment of late-onset nonketotic hyperglycinaemia: Effectiveness of imipramine and benzoateWiltshire, E.; Poplawski, N.; Harrison, R.; Fletcher, J.
2000Ornithine carbamoyltransferase deficiency presenting with chorea in a femaleWiltshire, E.; Poplawski, N.; Harbord, M.; Harrison, R.; Fletcher, J.
2000Carbohydrate-deficient glycoprotein syndrome: Beyond the screenFletcher, J.; Matthijs, G.; Jaeken, J.; Van Schaftingen, E.; Nelson, P.
2000Molecular cloning and characterisation of GPR74 a novel G-protein coupled receptor closest related to the Y-receptor familyParker, R.; Copeland, N.; Eyre, H.; Liu, M.; Gilbert, D.; Crawford, J.; Couzens, M.; Sutherland, G.; Jenkins, N.; Herzog, H.
2000Identification of a mutation in the XNP/ATR-X gene in a family reported as Smith-Fineman-Myers syndromeVillard, L.; Fontes, M.; Ades, L.; Gecz, J.
2000Association between parental perception of children's vulnerability to illness and management of children's asthmaSpurrier, N.; Sawyer, M.; Staugas, R.; Martin, A.; Kennedy, D.; Streiner, D.