E. Craft

Hypertelorism, radial ray defects, dextrocardia, hypoplastic ribs and renal anomaly: report of a second case and confirmation of the phenotype.

M. Suri, P. Vasudevan, G. Tanteles, 2012, Clinical dysmorphology.

Supporting families with Cancer: A patient centred survivorship model of care

J. Barwell, A. Cashmore, Elizabeth King, 2015, Familial Cancer.

Status epilepsy in CCM with KRIT1 gene change.

P. Vasudevan, E. Craft, Pradeep C Vasudevan, 2014, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

14q22.3 Microdeletion encompassing OTX2 in a five-generation family with microphthalmia, pituitary abnormalities, and intellectual disability

L. Cresswell, P. Vasudevan, P. Warman, 2016, Ophthalmic genetics.

3C syndrome

Y. Crow, E. Craft, C. Wildig, 2010, American journal of medical genetics. Part A.

Refining the Primrose syndrome phenotype: A study of five patients with ZBTB20 de novo variants and a review of the literature

K. Lachlan, M. Parker, S. Sharif, 2019, American journal of medical genetics. Part A.