Hidden mutations in cornelia de lange syndrome limitations of sanger sequencing in molecular diagnostics [Human Mutation, 36, (2014) 26-29]

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Persistent URL	doi.org/10.1002/humu.22755, hdl.handle.net/1765/82810
Journal	Human Mutation
Organisation	Biophysical Genomics, Department Cell Biology & Genetics
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	Braunholz, D., Obieglo, C., Parenti, I., Pozojevic, J., Eckhold, J., Reiz, B., Brænne, I., Wendt, K., Watrin, E., Vodopiutz, J., Rieder, H., Gillessen-Kaesbach, G.& Kaiser, F. (2015). Hidden mutations in cornelia de lange syndrome limitations of sanger sequencing in molecular diagnostics [Human Mutation, 36, (2014) 26-29]. Human Mutation, 36(2), 279–280.https://doi.org/10.1002/humu.22755

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