K. McKenzie

Multiple Congenital Melanocytic Nevi and Neurocutaneous Melanosis Are Caused by Postzygotic Mutations in Codon 61 of NRAS

N. Sebire, E. Healy, V. Kinsler, 2013, The Journal of investigative dermatology.

Germ cell differentiation in the marmoset (Callithrix jacchus) during fetal and neonatal life closely parallels that in the human

R. Sharpe, P. Saunders, W. Wallace, 2008, Human reproduction.

Subcutaneous panniculitic T-cell lymphoma in childhood: successful response to chemotherapy.

W. Wallace, A. Thomson, K. McKenzie, 2001, Medical and pediatric oncology.

Ten years of neonatal autopsies in tertiary referral centre: retrospective study

M. Brodlie, I. Laing, J. Keeling, 2002, BMJ : British Medical Journal.

Infantile choriocarcinoma treated with chemotherapy alone.

M. Seckl, W. Wallace, P. Crofton, 2003, Medical and pediatric oncology.

Mutations in COPA lead to abnormal trafficking of STING to the Golgi and interferon signaling

T. Molina, Y. Crow, J. Marsh, 2020, The Journal of experimental medicine.

Miller (Genee-Wiedemann) syndrome represents a clinically and biochemically distinct subgroup of postaxial acrofacial dysostosis associated with partial deficiency of DHODH.

C. Mercer, D. Wieczorek, Harris Morrison, 2012, Human molecular genetics.

In a Genomic Era, Placental Pathology Still Holds the Key in the Nondysmorphic Stillbirth

M. Porteous, M. Evans, K. McKenzie, 2018, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

DEMONSTRATION OF RENIN GENE EXPRESSION IN NEPHROBLASTOMA BY IN SITU HYBRIDIZATION

R. Ferrier, G. Lindop, K. McKenzie, 1996, Journal of Pathology.

Demonstration of Insulin production and storage in insulinomas by in situ hybridisation and immunocytochemistry

A. Foulis, M. Farquharson, K. McKenzie, 1997, Journal of Pathology.