Browsing by Author Rogers, Carolyn

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Issue DateTitleAuthor(s)Citation
2010CASK mutations are frequent in males and cause X-linked nystagmus and variable XLMR phenotypesGrigg, John; Wilson, Meredith; Boyle, Jackie; Cox, James; et al, various; Hackett, A; Licata, Andrea; Partington, Michael; Rogers, Carolyn; Stevenson, Roger; Tarpey, Patrick; Tolmie, John; Whibley, Annabel; Central Clinical School: Clinical Ophthal & Eye Health; Children's Hospital Westmead: Paediatrics & Child HealthCASK mutations are frequent in males and cause X-linked nystagmus and variable XLMR phenotypes, European Journal of Human Genetics, vol.18, 5,pp 544-552
2017Erratum: Hwang Y.T. et al. Molecular Inconsistencies in a Fragile X Male with Early Onset Ataxia. Genes 2016, 7, 68Heard, Robert; Aliaga, Solange Mabel; Arpone, Marta; Bretherton, Lesley; Dudding, Tracy E.; et al, Various; Francis, David; Hwang, Yun Tae; Li, Xin; Rogers, Carolyn; Slater, Howard Robert; Western Clinical School: Medicine (Westmead)Erratum: Hwang Y.T. et al. Molecular Inconsistencies in a Fragile X Male with Early Onset Ataxia. Genes 2016, 7, 68, Genes, vol.8, 2, 2017,pp 1-2
2013Maternal attitudes to newborn screening for fragile X syndromeBennetts, Bruce; Wiley, Veronica; Boyle, Jackie; Christie, Louise; Field, Michael; Goel, Himanshu; Hansen, Jessica; Hunter, Matthew; Rogers, Carolyn; Turner, Catherine; Wilcken, Bridget; Wotton, Tiffany; Children's Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Paediatrics & Child HealthMaternal attitudes to newborn screening for fragile X syndrome, American Journal of Medical Genetics. Part A, vol.161A, 2, 2013,pp 301-311
2016Molecular Inconsistencies in a Fragile X Male with Early Onset AtaxiaHeard, Robert; Aliaga, Solange Mabel; Arpone, Marta; Bretherton, Lesley; du Sart, Desiree; Dudding, Tracy E.; Francis, David; Godler, David; Hwang, Yun Tae; Li, Xin; Rogers, Carolyn; Slater, Howard Robert; Western Clinical School: Medicine (Westmead)Molecular Inconsistencies in a Fragile X Male with Early Onset Ataxia, Genes, vol.7, 9, 2016,pp 1-8