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Duerinckx S, Désir J, Perazzolo C, et al. Phenotypes and genotypes in non-consanguineous and consanguineous primary microcephaly: High incidence of epilepsy. Mol Genet Genomic Med. 2021;9(9):e1768doi: 10.1002/mgg3.1768.
Duerinckx, S., Désir, J., Perazzolo, C., Badoer, C., Jacquemin, V., Soblet, J., Maystadt, I., Tunca, Y., Blaumeiser, B., Ceulemans, B., Courtens, W., Debray, F. G., Destree, A., Devriendt, K., Jansen, A., Keymolen, K., Lederer, D., Loeys, B., Meuwissen, M., Moortgat, S., Mortier, G., Nassogne, M. C., Sekhara, T., Van Coster, R., Van Den Ende, J., Van der Aa, N., Van Esch, H., Vanakker, O., Verhelst, H., Vilain, C., Weckhuysen, S., Passemard, S., Verloes, A., Aeby, A., Deconinck, N., Van Bogaert, P., Pirson, I., & Abramowicz, M. (2021). Phenotypes and genotypes in non-consanguineous and consanguineous primary microcephaly: High incidence of epilepsy. Molecular genetics & genomic medicine, 9(9), e1768. https://doi.org/10.1002/mgg3.1768
Duerinckx, Sarah, et al. "Phenotypes and genotypes in non-consanguineous and consanguineous primary microcephaly: High incidence of epilepsy." Molecular genetics & genomic medicine vol. 9,9 (2021): e1768. doi: https://doi.org/10.1002/mgg3.1768
Duerinckx S, Désir J, Perazzolo C, Badoer C, Jacquemin V, Soblet J, Maystadt I, Tunca Y, Blaumeiser B, Ceulemans B, Courtens W, Debray FG, Destree A, Devriendt K, Jansen A, Keymolen K, Lederer D, Loeys B, Meuwissen M, Moortgat S, Mortier G, Nassogne MC, Sekhara T, Van Coster R, Van Den Ende J, Van der Aa N, Van Esch H, Vanakker O, Verhelst H, Vilain C, Weckhuysen S, Passemard S, Verloes A, Aeby A, Deconinck N, Van Bogaert P, Pirson I, Abramowicz M. Phenotypes and genotypes in non-consanguineous and consanguineous primary microcephaly: High incidence of epilepsy. Mol Genet Genomic Med. 2021 Sep;9(9):e1768. doi: 10.1002/mgg3.1768. Epub 2021 Aug 17. PMID: 34402213; PMCID: PMC8457702.
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