S. Knight

Clinical and molecular delineation of the 17q21.31 microdeletion syndrome

L. Vissers, B. D. de Vries, E. Eichler, 2008, Journal of Medical Genetics.

Del(18p) shown to be a cryptic translocation using a multiprobe FISH assay for subtelomeric chromosome rearrangements.

J. Flint, S. Knight, L. Kearney, 1998, Journal of medical genetics.

Submicroscopic 8pter deletion, mild mental retardation, and behavioral problems caused by a familial t(8;20)(p23;p13).

R. Regan, J. Flint, R. Winter, 2001, American journal of medical genetics.

Sixteen New Cases Contributing to the Characterization of Patients with Distal 22q11.2 Microduplications

B. V. van Bon, E. Bongers, D. Newbury, 2011, Molecular Syndromology.