Fiona Stewart

Clinical, MRI, and pathological features of polymicrogyria in chromosome 22q11 deletion syndrome

Renzo Guerrini, László Sztriha, B. Harding, 2004, American journal of medical genetics. Part A.

A specific mutation in TBL1XR1 causes Pierpont syndrome

Francesca Forzano, G Bradley Schaefer, Aldo Jongejan, 2016, Journal of Medical Genetics.

Association of mutation position in polycystic kidney disease 1 (PKD1) gene and development of a vascular phenotype

Jeffrey M Slezak, E. Bergstralh, F. Stewart, 2003, The Lancet.