Guidelines for the genetic diagnosis of hereditary recurrent fevers von Shinar, Y, Obici, L, Aksentijevich, I, Bennetts, B, Austrup, F, Ceccherini, I, Costa, J M, De Leener, A, Gattorno, M, Kania, U, Kone-Paut, I, Lezer, S, Livneh, A, Moix, I, Nishikomori, R, Ozen, S, Phylactou, L, Risom, L, Rowczenio, D, Sarkisian, T, van Gijn, M E, Witsch-Baumgartner, M, Morris, M, Hoffman, H M, Touitou, I

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New mutations in GJA8 expand the phenotype to include total sclerocornea von Ma, A.S., Grigg, J.R., Prokudin, I., Flaherty, M., Bennetts, B., Jamieson, R.V.

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Contiguous gene deletion syndrome in a female with ornithine transcarbamylase deficiency von Balasubramaniam, S., Rudduck, C., Bennetts, B., Peters, G., Wilcken, B., Ellaway, C.

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FBN1, TGFBR1, and the Marfan-craniosynostosis/mental retardation disorders revisited von Adès, L.C., Sullivan, K., Biggin, A., Haan, E.A., Brett, M., Holman, K.J., Dixon, J., Robertson, S., Holmes, A.D., Rogers, J., Bennetts, B.

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HIV-1 infection in an individual homozygous for the CCR5 deletion allele von Biti, Robyn, Ffrench, Rosemary, Young, Judy, Bennetts, Bruce, Stewart, Graeme, Liang, Tong

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Paraoxonase gene cluster is a genetic marker for early microvascular complications in Type 1 diabetes von Kao, Y., Donaghue, K. C., Chan, A., Bennetts, B. H., Knight, J., Silink, M.

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The association of aldose reductase gene (AKR1B1) polymorphisms with diabetic neuropathy in adolescents von Donaghue, K. C., Margan, S. H., Chan, A. K. F., Holloway, B., Silink, M., Rangel, T., Bennetts, B.

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A genome screen for linkage in Australian sibling-pairs with multiple sclerosis von Ban, M, Stewart, G J, Bennetts, B H, Heard, R, Simmons, R, Maranian, M, Compston, A, Sawcer, S J

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Anorexia nervosa (restrictive subtype) is associated with a polymorphism in the novel norepinephrine transporter gene promoter polymorphic region von URWIN, R. E, BENNETTS, B, WILCKEN, B, LAMPROPOULOS, B, BEUMONT, P, CLARKE, S, RUSSELL, J, TANNER, S, NUNN, K. P

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Temperature dependence of human muscle ClC-1 chloride channel von Bennetts, B., Roberts, M. L., Bretag, A. H., Rychkov, G. Y.

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Quality standards for DNA sequence variation databases to improve clinical management under development in Australia von Bennetts, B., Caramins, M., Hsu, A., Lau, C., Mead, S., Meldrum, C., Smith, T.D., Suthers, G., Taylor, G.R., Cotton, R.G.H., Tyrrell, V.

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Outcomes of Clinical Genetic Testing in Congenital Heart Disease – A Single-Site Audit Study von Morrish, A., O’Malley, B., Hilton, D., Sholler, G., Bennetts, B., Smith, J., Blue, G.

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Outcomes of Clinical Genetic Testing in Congenital Heart Disease – A Single-Site Audit Study von Morrish, A., O'Malley, B., Hilton, D., Sholler, G., Bennetts, B., Smith, J., Blue, G.

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Association of common T cell activation gene polymorphisms with multiple sclerosis in Australian patients von Teutsch, Suzy M., Booth, David R., Bennetts, Bruce H., Heard, Robert N.S., Stewart, Graeme J.

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An investigation of polymorphisms in the 4q13.3-21.1 CXC chemokine gene cluster for association with multiple sclerosis in Australians von Bugeja, M J, Booth, D R, Bennetts, B H, Heard, R NS, Stewart, G J

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Fast and Slow Gating of CLC-1: Differential Effects of 2-(4-Chlorophenoxy) Propionic Acid and Dominant Negative Mutations von Aromataris, E C, Rychkov, G Y, Bennetts, B, Hughes, B P, Bretag, A H, Roberts, M L

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A genome-wide screen for linkage disequilibrium in Australian HLA-DRB11501 positive multiple sclerosis patients von Ban, M., Sawcer, S.J., Heard, R.N.S., Bennetts, B.H., Adams, S., Booth, D., Perich, V., Setakis, E., Compston, A., Stewart, G.J.

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Lesch–Nyhan disease in a 20‐year‐ old man incorrectly described as developing ‘cerebral palsy’ after general anaesthesia in infancy von Chiong, M. A., Marinaki, A., Duley, J., Bennetts, B., Ouvrier, R., Christodoulou, J.

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Mutations of CDKL5 Cause a Severe Neurodevelopmental Disorder with Infantile Spasms and Mental Retardation von Weaving, Linda S., Christodoulou, John, Williamson, Sarah L., Friend, Kathie L., McKenzie, Olivia L.D., Archer, Hayley, Evans, Julie, Clarke, Angus, Pelka, Gregory J., Tam, Patrick P.L., Watson, Catherine, Lahooti, Hooshang, Ellaway, Carolyn J., Bennetts, Bruce, Leonard, Helen, Gécz, Jozef

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Looking different, feeling different: women’s reactions to risk-reducing breast and ovarian surgery von Hallowell, Nina, Baylock, Brandi, Heiniger, Louise, Butow, Phyllis N., Patel, Deepa, Meiser, Bettina, Saunders, Christobel, Price, Melanie A.

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