P. Finnegan

Osteoprotegerin deficiency and juvenile Paget's disease.

M. Podgornik, W. Mcalister, S. Mumm, 2002, The New England journal of medicine.

Denaturing gradient gel electrophoresis analysis of the tissue nonspecific alkaline phosphatase isoenzyme gene in hypophosphatasia.

M. Podgornik, P. Henthorn, S. Mumm, 2002, Molecular genetics and metabolism.

Historical Vignette: Hypophosphatasia: Molecular Diagnosis of Rathbun's Original Case

S. Mumm, M. Whyte, P. Finnegan, 2001, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

A five-base pair deletion in the sedlin gene causes spondyloepiphyseal dysplasia tarda in a six-generation Arkansas kindred.

B. Harding, R. Thakker, S. Mumm, 2000, The Journal of clinical endocrinology and metabolism.

Long-Acting Bronchodilator Therapy for the Treatment of Chronic Obstructive Pulmonary Disease

S. Bollmeier, P. Finnegan, A. Chen, 2008, The Annals of pharmacotherapy.