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Andrology|December 21, 2013
Cellular evidence for selfish spermatogonial selection in aged human testesG J Maher, A Goriely, A O M WilkieThe British Journal of Dermatology|April 20, 2007
Fibroblast growth factor receptor 3 (FGFR3) mutation in a verrucous epidermal naevus associated with mild facial dysmorphismB Collin, I B Taylor, A O M Wilkie, et al.Journal of Medical Genetics|May 12, 2009
Genetic screening of 202 individuals with congenital limb malformations and requiring reconstructive surgeryD Furniss, S-H Kan, I B Taylor, et al.American Journal of Human Genetics|August 2, 2007
A new subtype of brachydactyly type B caused by point mutations in the bone morphogenetic protein antagonist NOGGINK Lehmann, P Seemann, F Silan, et al.European Journal of Human Genetics : EJHG|November 28, 2013
Phenotypes of craniofrontonasal syndrome in patients with a pathogenic mutation in EFNB1M E P van den Elzen, S R F Twigg, J A C Goos, et al.Clinical Genetics|December 27, 2015
Acromelic frontonasal dysostosis and ZSWIM6 mutation: phenotypic spectrum and mosaicismS R F Twigg, L B Ousager, K A Miller, et al.Clinical Genetics|April 29, 2005
Molecular screening for microdeletions at 9p22-p24 and 11q23-q24 in a large cohort of patients with trigonocephalyF S Jehee, D Johnson, L G Alonso, et al.Journal of Medical Genetics|July 17, 2008
Clinical and molecular delineation of the 17q21.31 microdeletion syndromeD A Koolen, A J Sharp, J A Hurst, et al.Pageof 1