Abigail Woodroffe

A case of autism with an interstitial deletion on 4q leading to hemizygosity for genes encoding for glutamine and glycine neurotransmitter receptor sub-units (AMPA 2, GLRA3, GLRB) and neuropeptide receptors NPY1R, NPY5R

M. Spence, A. Woodroffe, Moyra J. Smith, 2004, BMC Medical Genetics.

Molecular genetic delineation of a deletion of chromosome 13q12→q13 in a patient with autism and auditory processing deficits

T. Laulhere, J. Martinez, C. Modahl, 2003, Cytogenetic and Genome Research.