Bad bones, absent smell, selfish testes: the pleiotropic consequences of human FGF receptor mutations. by Wilkie, A

Pitfalls in the phylogenomic evaluation of human disease-causing mutations. by Wilkie, A

Why study human limb malformations? by Wilkie, A

Cancer drugs to treat birth defects. by Wilkie, A

New insights into craniofacial malformations. by Twigg, S, Wilkie, A

A genetic-pathophysiological framework for craniosynostosis by Twigg, S, Wilkie, A

Clinical hypochondroplasia in a family caused by a heterozygous double mutation in FGFR3 encoding GLY380LYS. by Santos, H, Almeida, M, Fernandes, H, Wilkie, A, Wilkie, A

Paternal age effect mutations and selfish spermatogonial selection: causes and consequences for human disease. by Goriely, A, Wilkie, A

The genetics of mental retardation. by Flint, J, Wilkie, A

Gonadal mosaicism and non-invasive prenatal diagnosis for "reassurance" in sporadic paternal age effect (PAE) disorders by Goriely, A, Wilkie, A

Genetic aspects of birth defects: new understandings of old problems. by Prescott, K, Wilkie, A

Missing heritability: paternal age effect mutations and selfish spermatogonia. by Goriely, A, Wilkie, A

Enlarged parietal foramina by Mavrogiannis, L, Wilkie, A

Genetic aspects of birth defects: New understandings of old problems by Prescott, K, Wilkie, A

Craniosynostosis by Johnson, D, Wilkie, A

The rational points of a definable set by Pila, J, Wilkie, A

Clinical genetics of craniosynostosis by Wilkie, A, Johnson, D, Wall, S

Growth of the normal skull vault and its alteration in craniosynostosis: insights from human genetics and experimental studies. by Morriss-Kay, G, Wilkie, A

Efficient use of a 'dead-end' GA 5' splice site in the human fibroblast growth factor receptor genes. by Brackenridge, S, Wilkie, A, Screaton, G

Cellular evidence for selfish spermatogonial selection in aged human testes by Maher, G, Goriely, A, Wilkie, A