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2 Publications
2018 | Journal Article | IST-REx-ID: 691 | 
A homozygous founder mutation in TRAPPC6B associates with a neurodevelopmental disorder characterised by microcephaly epilepsy and autistic features
I. Marin Valencia, G. Novarino, A. Johansen, B. Rosti, M. Issa, D. Musaev, G. Bhat, E. Scott, J. Silhavy, V. Stanley, R. Rosti, J. Gleeson, F. Imam, M. Zaki, J. Gleeson, Journal of Medical Genetics 55 (2018) 48–54.
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| PubMed | Europe PMC
I. Marin Valencia, G. Novarino, A. Johansen, B. Rosti, M. Issa, D. Musaev, G. Bhat, E. Scott, J. Silhavy, V. Stanley, R. Rosti, J. Gleeson, F. Imam, M. Zaki, J. Gleeson, Journal of Medical Genetics 55 (2018) 48–54.
1983 | Book Chapter | IST-REx-ID: 4328
Hybrid zones as barriers to gene flow
N.H. Barton, G. Hewitt, in:, G. Oxford, D. Rollinson (Eds.), Protein Polymorphism: Adaptive and Taxonomic Significance, Academic Press, 1983, pp. 341–359.
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N.H. Barton, G. Hewitt, in:, G. Oxford, D. Rollinson (Eds.), Protein Polymorphism: Adaptive and Taxonomic Significance, Academic Press, 1983, pp. 341–359.