C. McMahon

Possible evidence for genomic imprinting in childhood acute myeloblastic leukaemia associated with monosomy for chromosome 7

J. Chessells, B. Reeves, F. Katz, 1992, British journal of haematology.

A case of myopathy associated with a dystrophin gene deletion and abnormal glycogen storage

M. Rose, J. Morgan-Hughes, S. Genet, 1993, Muscle & nerve.

B-cell-negative severe combined immunodeficiency associated with a common γ chain mutation

P. Clark, C. Kinnon, S. Genet, 1997, Human Genetics.

Human IFNAR2 deficiency: Lessons for antiviral immunity

T. Jacques, M. Hubank, J. Breuer, 2015, Science Translational Medicine.

The major cystic fibrosis mutation in a British population

M. Pembrey, S. Malcolm, H. Middleton-Price, 1990, Human Genetics.

Successful Treatment of Refractory Cardiac Arrest With β-Blockade and Extracorporeal Life Support in a Pediatric Patient With Catecholaminergic Polymorphic Ventricular Tachycardia: A Case Report.

C. McMahon, A. Cafferkey, 2018, A&A practice.