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Investigation of abnormal methylation and the CGG repeat expansion of the FMR-1 gene in familial autism and in cases autism with low level fragile X expression

Gurling, HMD; Vincent, J; Melmer, G; Bolton, P; Hodgkinson, S; Holmes, D; Lord, C; (1997) Investigation of abnormal methylation and the CGG repeat expansion of the FMR-1 gene in familial autism and in cases autism with low level fragile X expression. Human Heredity , 222 pp. 254-262.

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Type: Article
Title: Investigation of abnormal methylation and the CGG repeat expansion of the FMR-1 gene in familial autism and in cases autism with low level fragile X expression
Keywords: EXPRESSION, FAMILIAL, GENE, LEVEL
UCL classification: UCL > Provost and Vice Provost Offices
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > Division of Psychiatry
URI: http://discovery.ucl.ac.uk/id/eprint/89027
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