D. Morris

The Allergist's Role in Detection of Severe Alpha-1 Antitrypsin Deficiency.

T. Kelbel, T. Craig, M. Henao, 2017, The journal of allergy and clinical immunology. In practice.

Adult-onset arginase deficiency

D. Cowley, J. V. van Dongen, J. Mcgill, 1998, Journal of Inherited Metabolic Disease.

Congenital disorder of glycosylation type 1a: Three siblings with a mild neurological phenotype

D. Appleton, J. Jaeken, J. Mcgill, 2007, Journal of Clinical Neuroscience.

Evaluation of the Technicon Immuno 1 free thyroxine assay.

D. Ehresman, J. Bock, Jeanette D. Cheng, 1996, American journal of clinical pathology.

Congenital disorder of glycosylation type Ia in a 6-year-old girl with a mild intellectual phenotype: Two novel PMM2 mutations

J. Mcgill, D. Coman, S. Klingberg, 2005, Journal of Inherited Metabolic Disease.

Deficiency of respiratory chain complex I is a common cause of leigh disease

D. Turnbull, G. Brown, B. Harding, 1996, Annals of neurology.