Mutation update on the CHD7 gene involved in CHARGE syndrome
Janssen, Nicole, Bergman, Jorieke E. H., Swertz, Morris A., Tranebjaerg, Lisbeth, Lodahl, Marianne, Schoots, Jeroen, Hofstra, Robert M. W., van Ravenswaaij-Arts, Conny M. A., Hoefsloot, Lies H.
Published in Human mutation (01.08.2012)
Published in Human mutation (01.08.2012)
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Data-driven directions for effective footwear provision for the high-risk diabetic foot
Arts, M. L. J., de Haart, M., Waaijman, R., Dahmen, R., Berendsen, H., Nollet, F., Bus, S. A.
Published in Diabetic medicine (01.06.2015)
Published in Diabetic medicine (01.06.2015)
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Rapid Targeted Genomics in Critically Ill Newborns
van Diemen, Cleo C, Kerstjens-Frederikse, Wilhelmina S, Bergman, Klasien A, de Koning, Tom J, Sikkema-Raddatz, Birgit, van der Velde, Joeri K, Abbott, Kristin M, Herkert, Johanna C, Löhner, Katharina, Rump, Patrick, Meems-Veldhuis, Martine T, Neerincx, Pieter B T, Jongbloed, Jan D H, van Ravenswaaij-Arts, Conny M, Swertz, Morris A, Sinke, Richard J, van Langen, Irene M, Wijmenga, Cisca
Published in Pediatrics (Evanston) (01.10.2017)
Published in Pediatrics (Evanston) (01.10.2017)
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Normal values for quantitative muscle ultrasonography in adults
Arts, Ilse M.P., Pillen, Sigrid, Schelhaas, H. Jurgen, Overeem, Sebastiaan, Zwarts, Machiel J.
Published in Muscle & nerve (01.01.2010)
Published in Muscle & nerve (01.01.2010)
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CHD7 mutations and CHARGE syndrome: the clinical implications of an expanding phenotype
Bergman, J E H, Janssen, N, Hoefsloot, L H, Jongmans, M C J, Hofstra, R M W, van Ravenswaaij-Arts, C M A
Published in Journal of Medical Genetics (01.05.2011)
Published in Journal of Medical Genetics (01.05.2011)
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Book Review
CHD7, the gene mutated in CHARGE syndrome, regulates genes involved in neural crest cell guidance
Schulz, Yvonne, Wehner, Peter, Opitz, Lennart, Salinas-Riester, Gabriela, Bongers, Ernie M. H. F., van Ravenswaaij-Arts, Conny M. A., Wincent, Josephine, Schoumans, Jacqueline, Kohlhase, Jürgen, Borchers, Annette, Pauli, Silke
Published in Human genetics (01.08.2014)
Published in Human genetics (01.08.2014)
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