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2 Publications
2018 | Journal Article | IST-REx-ID: 691 | 
Marin Valencia I, Novarino G, Johansen A, Rosti B, Issa M, Musaev D, Bhat G, Scott E, Silhavy J, Stanley V, Rosti R, Gleeson J, Imam F, Zaki M, Gleeson J. 2018. A homozygous founder mutation in TRAPPC6B associates with a neurodevelopmental disorder characterised by microcephaly epilepsy and autistic features. Journal of Medical Genetics. 55(1), 48–54.
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| PubMed | Europe PMC
1983 | Book Chapter | IST-REx-ID: 4328
Barton NH, Hewitt G. 1983.Hybrid zones as barriers to gene flow. In: Protein polymorphism: Adaptive and taxonomic significance. Systematics Association Special Volume, vol. 24, 341–359.
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