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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., … 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. BMJ Publishing Group. https://doi.org/10.1136/jmedgenet-2017-104627
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| PubMed | Europe PMC
1983 | Book Chapter | IST-REx-ID: 4328
Barton, N. H., & Hewitt, G. (1983). Hybrid zones as barriers to gene flow. In G. Oxford & D. Rollinson (Eds.), Protein polymorphism: Adaptive and taxonomic significance (Vol. 24, pp. 341–359). University of York, United Kingdom: Academic Press.
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