Publications by authors named "Deirdre Cilliers"

17Publications

The Significance of Squamosal Suture Synostosis.

J Craniofac Surg 2016 Sep;27(6):1543-9

*Oxford Craniofacial Unit, West Wing †Department of Neuroradiology, John Radcliffe Hospital, Oxford, UK.

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http://dx.doi.org/10.1097/SCS.0000000000002888DOI Listing
September 2016

Genetic heterogeneity in Cornelia de Lange syndrome (CdLS) and CdLS-like phenotypes with observed and predicted levels of mosaicism.

J Med Genet 2014 Oct 14;51(10):659-68. Epub 2014 Aug 14.

MRC Human Genetics Unit, MRC Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, UK.

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http://dx.doi.org/10.1136/jmedgenet-2014-102573DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4173748PMC
October 2014

A new X-linked mental retardation (XLMR) syndrome with late-onset primary testicular failure, short stature and microcephaly maps to Xq25-q26.

Eur J Med Genet 2007 May-Jun;50(3):216-23. Epub 2007 Jan 27.

Academic Department of Medical Genetics and Regional Genetic Services, St Mary's Hospital, University of Manchester, Manchester, UK.

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http://dx.doi.org/10.1016/j.ejmg.2007.01.003DOI Listing
July 2007

Cerebro-facio-thoracic dysplasia: expanding the phenotype.

Clin Dysmorphol 2007 Apr;16(2):121-5

Academic Department of Medical Genetics and Regional Genetics Service, St Mary's Hospital, University of Manchester, Manchester, UK.

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http://dx.doi.org/10.1097/MCD.0b013e328012e292DOI Listing
April 2007