A. Jolley

Novel protein C gene mutation in a compound heterozygote resulting in catastrophic thrombosis in early adulthood: diagnosis and long‐term treatment with subcutaneous protein C concentrate

A. Gallus, Nancy V Lerda, D. M. Ross, 2016, British journal of haematology.

De novo intragenic deletion of the autism susceptibility candidate 2 (AUTS2) gene in a patient with developmental delay: A case report and literature review

M. Corbett, Sui Yu, J. Nicholl, 2013, American journal of medical genetics. Part A.

Magnetic resonance imaging in the diagnosis of suspected cornual pregnancy. A case report.

K. Fogarty, A. Jolley, C. Lee, 1995, The Journal of reproductive medicine.

Intrauterine Fetal Death With Vanishing Gastroschisis and Post Mortem Examination Findings

L. Moore, P. Muller, C. Cord-Udy, 2017, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Phenotypic variation of TTC19‐deficient mitochondrial complex III deficiency: A case report and literature review

K. Friend, A. Compton, S. Balasubramaniam, 2015, American journal of medical genetics. Part A.