Publications by Dr Arjan De Brouwer - ePrints

Newcastle Authors	Title	Year
Dr Tara Montgomery Dr Miranda Splitt Dr Arjan De Brouwer	De novo and biallelic DEAF1 variants cause a phenotypic spectrum	2019
Dr Francesco Bruni Dr Kyle Thompson Dr Langping He Dr Arjan De Brouwer Professor Robert Taylor et al.	Confirming TDP2 mutation in spinocerebellar ataxia autosomal recessive 23 (SCAR23)	2018
Professor Robert Taylor Dr Arjan De Brouwer	Progressive deafness–dystonia due to SERAC1 mutations: A study of 67 cases	2017
Dr Arjan De Brouwer	Mutation Frequencies of X-linked Mental Retardation Genes in Families from the EuroMRX Consortium	2007
Dr Arjan De Brouwer Professor Joris Veltman	Chromosomal copy number changes in patients with non-syndromic X linked mental retardation detected by array CGH	2006