Gregory J. Fitzgibbon

Array comparative genomic hybridisation-based identification of two imbalances of chromosome 1p in a 9-year-old girl with a monosomy 1p36 related phenotype and a family history of learning difficulties: a case report

L. Gaunt, J. Clayton-Smith, M. Needham, 2008, Journal of medical case reports.

Genetic Analysis of the TOR Pathway in Aspergillus nidulans

M. Caddick, Meriel G. Jones, I. Morozov, 2005, Eukaryotic Cell.

A novel 800 kb microduplication of chromosome 16q22.1 resulting in learning disability and epilepsy may explain phenotypic variability in a family with 15q13 microdeletion

L. Gaunt, J. Clayton-Smith, S. Banka, 2011, American journal of medical genetics. Part A.

Haploinsufficiency of the nerve growth factor beta gene in a 1p13 deleted female child with an insensitivity to pain

L. Gaunt, M. Needham, H. Kingston, 2009, Developmental medicine and child neurology.