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Research Output 1996 2019

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Letter
2014
6 Citations (Scopus)

Whole genome sequencing identifies a novel occludin mutation in microcephaly with band-like calcification and polymicrogyria that extends the phenotypic spectrum

Elsaid, M. F., Kamel, H., Chalhoub, N., Aziz, N. A., Ibrahim, K., Ben-Omran, T., George, B., Aldous, E., Ali Mohamoud, Y., Malek, J., Ross, M. E. & Kamal Abd El Aleem, A., 2014, In : American Journal of Medical Genetics, Part A. 164, 6, p. 1614-1617 4 p.

Research output: Contribution to journalLetter

Occludin
Consanguinity
Malformations of Cortical Development
Calcinosis
Microcephaly