S. McKee

Clinical and radiologic findings in progressive facial hemiatrophy (Parry-Romberg syndrome).

R. Cory, D. Clayman, W. Faillace, 1997, AJNR. American journal of neuroradiology.

Evidence for digenic inheritance in some cases of Antley-Bixler syndrome?

D. Sillence, W. Reardon, P. Hindmarsh, 2000, Journal of medical genetics.

Pierpont Syndrome: A Collaborative Study

N. de Leeuw, W. Reardon, K. Devriendt, 2011, American journal of medical genetics. Part A.

SPECC1L Mutations Are Not Common in Sporadic Cases of Opitz G/BBB Syndrome

G. Meroni, F. Faravelli, P. Prontera, 2022, Genes.

A clinical study of Aicardi syndrome in Northern Ireland: the spectrum of ophthalmic findings

M. O'Keefe, S. McKee, E. McLoone, 2016, Eye.

Septo-optic dysplasia with a transverse limb defect.

S. McKee, A. Bell, A. Chillingworth, 2008, Clinical dysmorphology.

Correction to: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith–Magenis syndrome

J. Rosenfeld, E. Roeder, J. Lupski, 2019, Genome Medicine.