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Clumsiness, confusion, coma, and valproate.
Ellaway CJ, Bennetts B, Tuck RR, Wilcken B. Ellaway CJ, et al. Among authors: bennetts b. Lancet. 1999 Apr 24;353(9162):1408. doi: 10.1016/s0140-6736(99)01433-6. Lancet. 1999. PMID: 10227223 No abstract available.
Medium-chain acyl-CoA dehydrogenase deficiency: genotype-biochemical phenotype correlations.
Waddell L, Wiley V, Carpenter K, Bennetts B, Angel L, Andresen BS, Wilcken B. Waddell L, et al. Among authors: bennetts b. Mol Genet Metab. 2006 Jan;87(1):32-9. doi: 10.1016/j.ymgme.2005.09.020. Epub 2005 Nov 15. Mol Genet Metab. 2006. PMID: 16291504
Lesch-Nyhan disease in a 20-year- old man incorrectly described as developing 'cerebral palsy' after general anaesthesia in infancy.
Chiong MA, Marinaki A, Duley J, Bennetts B, Ouvrier R, Christodoulou J. Chiong MA, et al. Among authors: bennetts b. J Inherit Metab Dis. 2006 Aug;29(4):594. doi: 10.1007/s10545-006-0281-4. Epub 2006 Jul 6. J Inherit Metab Dis. 2006. PMID: 16826447
Contiguous gene deletion syndrome in a female with ornithine transcarbamylase deficiency.
Balasubramaniam S, Rudduck C, Bennetts B, Peters G, Wilcken B, Ellaway C. Balasubramaniam S, et al. Among authors: bennetts b. Mol Genet Metab. 2010 Jan;99(1):34-41. doi: 10.1016/j.ymgme.2009.08.007. Mol Genet Metab. 2010. PMID: 19783189
An investigation of NOS2A promoter polymorphisms in Australian multiple sclerosis patients.
Bugeja MJ, Booth DR, Bennetts BH, Heard RN, Burgner D, Stewart GJ. Bugeja MJ, et al. Among authors: bennetts bh. Eur J Hum Genet. 2005 Jul;13(7):815-22. doi: 10.1038/sj.ejhg.5201422. Eur J Hum Genet. 2005. PMID: 15856071 Free article.
An investigation of polymorphisms in the 17q11.2-12 CC chemokine gene cluster for association with multiple sclerosis in Australians.
Bugeja MJ, Booth D, Bennetts B, Heard R, Rubio J, Stewart G. Bugeja MJ, et al. Among authors: bennetts b. BMC Med Genet. 2006 Jul 26;7:64. doi: 10.1186/1471-2350-7-64. BMC Med Genet. 2006. PMID: 16872505 Free PMC article.
The clinical phenotype of mosaicism for genome-wide paternal uniparental disomy: two new reports.
Wilson M, Peters G, Bennetts B, McGillivray G, Wu ZH, Poon C, Algar E. Wilson M, et al. Among authors: bennetts b. Am J Med Genet A. 2008 Jan 15;146A(2):137-48. doi: 10.1002/ajmg.a.32172. Am J Med Genet A. 2008. PMID: 18033734
Autosomal recessive transmission of TRAPS in a family with a novel TNFRSF1A mutation.
Wong KK, Jackson J, Whidborne R, Mallon D, Bennetts B, D'Orsogna LJ. Wong KK, et al. Among authors: bennetts b. Scand J Rheumatol. 2015 May;44(3):255-6. doi: 10.3109/03009742.2015.1005663. Epub 2015 Mar 6. Scand J Rheumatol. 2015. PMID: 25744939 No abstract available.
Effects of MECP2 mutation type, location and X-inactivation in modulating Rett syndrome phenotype.
Weaving LS, Williamson SL, Bennetts B, Davis M, Ellaway CJ, Leonard H, Thong MK, Delatycki M, Thompson EM, Laing N, Christodoulou J. Weaving LS, et al. Among authors: bennetts b. Am J Med Genet A. 2003 Apr 15;118A(2):103-14. doi: 10.1002/ajmg.a.10053. Am J Med Genet A. 2003. PMID: 12655490
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