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Number of items: 3.

Cyganek, L., Hanses, U., Li, Y., Tiburcy, M., Barbarics, B., Yigit, G., Altmueller, J., Paul, T., Zimmermann, W. H., Hasenfuss, G. and Wollnik, B. (2018). Exploring hypertrophic cardiomyopathy in iPSC-derived cardiomyocytes from patients with a novel autosomal recessive form of Noonan syndrome. Eur. Heart J., 39. S. 1089 - 1090. OXFORD: OXFORD UNIV PRESS. ISSN 1522-9645

Moosa, S., Yamamoto, G. L., Garbes, L., Keupp, K., Beleza-Meireles, A., Moreno, C. A., Valadares, E. R., de Sousa, S. B., Maia, S., Saraiva, J., Honjo, R. S., Kim, C. A., Cabral de Menezes, H., Lausch, E., Lorini, P. V., Lamounier, A., Jr., Carniero, T. C. B., Giunta, C., Rohrbach, M., Janner, M., Semler, O., Beleggia, F., Li, Y., Yigit, G., Reintjes, N., Altmuller, J., Nurnberg, P., Cavalcanti, D. P., Zabel, B., Warman, M. L., Bertola, D. R., Wollnik, B. and Netzer, C. (2020). Severe Osteogenesis imperfecta with oligodontia: think of MESD. Eur. J. Hum. Genet., 28 (SUPPL 1). S. 248 - 250. LONDON: SPRINGERNATURE. ISSN 1476-5438

Yigit, G. and Wollnik, B. (2012). Molecular mechanisms underlying Seckel syndrome. Med. Genet., 24 (4). S. 284 - 289. HEIDELBERG: SPRINGER HEIDELBERG. ISSN 1863-5490

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