Browsing by Author Archer, Hayley L.

Jump to: 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
or enter first few letters:  
Showing results 1 to 3 of 3
Issue DateTitleAuthor(s)Citation
2006NTNG1 mutations are a rare cause of Rett syndrome.Christodoulou, John; Ravine, David; Archer, Hayley L.; Clarke, Angus; Evans, Julie C; Grove, Lucy; Kerr, Alison; Lazarou, Lazarus; Leonard, Helen; Millar, David S.; Pilz, Daniela T; Sampson, Julien; Thompson, Peter W.; Verity, Christopher; Whatley, Sharon; Children's Hospital Westmead: Paediatrics & Child Health; Medicine Faculty OfficeNTNG1 mutations are a rare cause of Rett syndrome., American journal of medical genetics Part A, vol.140A,(7),2006,pp 691-694
2005p.R270X MECP2 mutation and mortality in Rett syndromeChristodoulou, John; Archer, Hayley L.; Bailey, Mark E.S.; de Klerk, Nick; Jian, Le; Kerr, Alison; Laurvick, Crystal; Leonard, Helen; Ravine, David; Children's Hospital Westmead: Paediatrics & Child Healthp.R270X MECP2 mutation and mortality in Rett syndrome, European Journal of Human Genetics (2005), vol.13,(11),2005,pp 1235-1238
2012Transcription factor 4 and myocyte enhancer factor 2C mutations are not common causes of Rett syndromeArmani, Roksana; Christodoulou, John; Ho, Gladys; Archer, Hayley L.; Clarke, Angus; Cloosterman, Desiree; Vasudevan, Pradeep; Williamson, Sarah L; Yang, Nan; Zweier, Christiane; Children's Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Paediatrics & Child HealthTranscription factor 4 and myocyte enhancer factor 2C mutations are not common causes of Rett syndrome, American Journal of Medical Genetics. Part A, vol.158A, 4, 2012,pp 713-719