K. Sprysak

An HFE intronic variant promotes misdiagnosis of hereditary hemochromatosis.

M. Somerville, M. Hicks, K. Sprysak, 1999, American journal of human genetics.

Microduplication and triplication of 22q11.2: a highly variable syndrome.

L. Shaffer, M. Somerville, B. Morrow, 2005, American journal of human genetics.

Chromosome 1q21.1 Contiguous Gene Deletion Is Associated With Congenital Heart Disease

M. Somerville, J. S. Bamforth, J. Dyck, 2004, Circulation research.

Heteroduplex-based genotyping with microchip electrophoresis and dHPLC.

M. Somerville, C. Backhouse, R. Tomaszewski, 2003, Genetic testing.