Publications by authors named "Josie Innes"

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CNVs affecting cancer predisposing genes (CPGs) detected as incidental findings in routine germline diagnostic chromosomal microarray (CMA) testing.
Josie Innes, Lisa Reali, Jill Clayton-Smith, Georgina Hall, Derek Hk Lim

J Med Genet· February 2018

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Further Clinical Delineation of the MEF2C Haploinsufficiency Syndrome: Report on New Cases and Literature Review of Severe Neurodevelopmental Disorders Presenting with Seizures, Absent Speech, and Involuntary Movements.
Irena Vrečar, Josie Innes, Elizabeth A Jones, Helen Kingston, William Reardon

J Pediatr Genet· September 2017

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Mosaic structural variation in children with developmental disorders.
Daniel A King, Wendy D Jones, Yanick J Crow, Anna F Dominiczak, Nicola A Foster, Josie Innes

Hum Mol Genet· May 2015

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Interchromosomal insertional translocation at Xq26.3 alters SOX3 expression in an individual with XX male sex reversal.
Bryan Haines, James Hughes, Mark Corbett, Marie Shaw, Josie Innes

J Clin Endocrinol Metab· May 2015

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