Point mutations throughout the GLI3 gene cause Greig cephalopolysyndactyly syndrome

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Persistent URL	doi.org/10.1093/hmg/8.9.1769, hdl.handle.net/1765/55655
Journal	Human Molecular Genetics
Organisation	Department of Clinical Chemistry
Citation APA APA Style APA-ALL Style AAA Style Cell Style Chicago Style Harvard Style IEEE Style MLA Style Nature Style Vancouver Style American-Institute-of-Physics Style Council-of-Science-Editors Style BibTex Format Endnote Format RIS Format CSL Format DOIs only Format	Kalff-Suske, M., Wild, A., Topp, H., Wessling, M., Jacobsen, E.-M., Bornholdt, D., Engel, H., Heuer, H., Aalfs, C., Ausems, M., Barone, R., Herzog, A., Heutink, P., Homfray, T., Gillessen-Kaesbach, G., König, R., Kunze, J., Meinecke, P., Müller, D., … Grzeschik, K.-H. (1999). Point mutations throughout the GLI3 gene cause Greig cephalopolysyndactyly syndrome. Human Molecular Genetics, 8(9), 1769–1777.https://doi.org/10.1093/hmg/8.9.1769

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